메뉴 건너뛰기




Volumn 23, Issue 9, 2015, Pages 1116-1123

The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases

(35)  Mora, Marina a   Angelini, Corrado b,c   Bignami, Fabrizia d   Bodin, Anne Mary e   Crimi, Marco f   Di Donato, Jeanne Hélène g   Felice, Alex h   Jaeger, Cécile i   Karcagi, Veronika j   Lecam, Yann e   Lynn, Stephen k   Meznaric, Marija l   Moggio, Maurizio m   Monaco, Lucia f   Politano, Luisa n   De La Paz, Manuel Posada o   Saker, Safaa p   Schneiderat, Peter q   Ensini, Monica k   Garavaglia, Barbara a   more..


Author keywords

[No Author keywords available]

Indexed keywords

ACHIEVEMENT; ARTICLE; BIOBANKING; BIOINFORMATICS; CONCEPTUAL FRAMEWORK; DECISION MAKING; DISEASE REGISTRY; EUROBIOBANK NETWORK; EUROPEAN; HEALTH CARE FACILITY; HEALTH CARE ORGANIZATION; HUMAN; INFORMATION PROCESSING; INFORMATION TECHNOLOGY; INTERNATIONAL COOPERATION; PRIORITY JOURNAL; PROFESSIONAL STANDARD; PUBLICATION; QUALITY CONTROL; RARE DISEASE; TOTAL QUALITY MANAGEMENT; BIOBANK; BIOLOGY; EUROPE; GENETICS; ORGANIZATION AND MANAGEMENT; PATHOLOGY; RARE DISEASES; REGISTER;

EID: 84939265617     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2014.272     Document Type: Article
Times cited : (51)

References (51)
  • 1
    • 84939288448 scopus 로고    scopus 로고
    • OECD: Glossary of Statistical Terms
    • OECD: Glossary of Statistical Terms, 2006. Available at http://stats.oecd.org/glossary/ detail.asp?ID=7220.
    • (2006)
  • 2
    • 84883168131 scopus 로고    scopus 로고
    • Telethon Network of Genetic Biobanks: A key service for diagnosis and research on rare diseases
    • Filocamo M, Baldo C, Goldwurm S et al: Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases. Orphanet J Rare Dis 2013; 8: 129.
    • (2013) Orphanet J Rare Dis , vol.8 , pp. 129
    • Filocamo, M.1    Baldo, C.2    Goldwurm, S.3
  • 3
    • 41449117980 scopus 로고    scopus 로고
    • Biobanks: Transnational, European and global networks
    • Asslaber M, Zatloukal K: Biobanks: transnational, European and global networks. Brief Funct Genomic Proteomic 2007; 6: 193-201.
    • (2007) Brief Funct Genomic Proteomic , vol.6 , pp. 193-201
    • Asslaber, M.1    Zatloukal, K.2
  • 5
    • 84867741263 scopus 로고    scopus 로고
    • Toward a roadmap in global biobanking for health
    • Harris JR, Burton P, Knoppers BM et al: Toward a roadmap in global biobanking for health. Eur J Hum Genet 2012; 20: 1105-1111.
    • (2012) Eur J Hum Genet , vol.20 , pp. 1105-1111
    • Harris, J.R.1    Burton, P.2    Knoppers, B.M.3
  • 6
    • 77955869796 scopus 로고    scopus 로고
    • The role of biobanking in rare diseases: European consensus expert group report
    • Lochmüller H, Aymé S, Pampinella F: The role of biobanking in rare diseases: European consensus expert group report. Biopreserv Biobank 2009; 7: 155-156.
    • (2009) Biopreserv Biobank , vol.7 , pp. 155-156
    • Lochmüller, H.1    Aymé, S.2    Pampinella, F.3
  • 10
    • 27544494568 scopus 로고    scopus 로고
    • Complete loss-of-function of the heart/musclespecific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy
    • Palmieri L, Alberio S, Pisano I et al: Complete loss-of-function of the heart/musclespecific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy. Hum Mol Genet 2005; 14: 3079-3088.
    • (2005) Hum Mol Genet , vol.14 , pp. 3079-3088
    • Palmieri, L.1    Alberio, S.2    Pisano, I.3
  • 11
    • 33847176234 scopus 로고    scopus 로고
    • Mitochondrial phosphate-carrier deficiency: A novel disorder of oxidative phosphorylation
    • Mayr JA, Merkel O, Kohlwein SD et al: Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation. Am J Hum Genet 2007; 80: 478-484.
    • (2007) Am J Hum Genet , vol.80 , pp. 478-484
    • Mayr, J.A.1    Merkel, O.2    Kohlwein, S.D.3
  • 12
    • 77956622584 scopus 로고    scopus 로고
    • Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
    • Borg J, Papadopoulos P, Georgitsi M et al: Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin. Nat Genet 2010; 42: 733-734.
    • (2010) Nat Genet , vol.42 , pp. 733-734
    • Borg, J.1    Papadopoulos, P.2    Georgitsi, M.3
  • 13
    • 77954542018 scopus 로고    scopus 로고
    • The genome-wide structure of the Jewish people
    • Behar DM, Yunusbayev B, Metspalu M et al: The genome-wide structure of the Jewish people. Nature 2010; 466: 238-242.
    • (2010) Nature , vol.466 , pp. 238-242
    • Behar, D.M.1    Yunusbayev, B.2    Metspalu, M.3
  • 14
    • 80055068583 scopus 로고    scopus 로고
    • Motor chip: A comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders
    • Piluso G, Dionisi M, Del Vecchio Blanco F et al: Motor chip: a comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders. Clin Chem 2011; 57: 1584-1596.
    • (2011) Clin Chem , vol.57 , pp. 1584-1596
    • Piluso, G.1    Dionisi, M.2    Del Vecchio Blanco, F.3
  • 15
    • 78650702096 scopus 로고    scopus 로고
    • Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency
    • Kemp JP, Smith PM, Pyle A et al: Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency. Brain 2011; 134: 183-195.
    • (2011) Brain , vol.134 , pp. 183-195
    • Kemp, J.P.1    Smith, P.M.2    Pyle, A.3
  • 16
    • 79851494905 scopus 로고    scopus 로고
    • Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect
    • Senderek J, Müller JS, Dusl M et al: Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect. Am J Hum Genet 2011; 88: 162-172.
    • (2011) Am J Hum Genet , vol.88 , pp. 162-172
    • Senderek, J.1    Müller, J.S.2    Dusl, M.3
  • 17
    • 84866063186 scopus 로고    scopus 로고
    • Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause for Walker-Warburg Syndrome
    • Manzini C, Tambunan DE, Hill RS et al: Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause for Walker-Warburg Syndrome. Am J Hum Genet 2012; 91: 541-547.
    • (2012) Am J Hum Genet , vol.91 , pp. 541-547
    • Manzini, C.1    Tambunan, D.E.2    Hill, R.S.3
  • 18
    • 84866252725 scopus 로고    scopus 로고
    • Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
    • Bello L, Piva L, Barp A et al: Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Neurology 2012; 79: 159-162.
    • (2012) Neurology , vol.79 , pp. 159-162
    • Bello, L.1    Piva, L.2    Barp, A.3
  • 19
    • 84884258121 scopus 로고    scopus 로고
    • Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome
    • Cozzi A, Santambrogio P, Privitera D et al: Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome. J Exp Med 2013; 210: 1779-1791.
    • (2013) J Exp Med , vol.210 , pp. 1779-1791
    • Cozzi, A.1    Santambrogio, P.2    Privitera, D.3
  • 20
    • 84891835067 scopus 로고    scopus 로고
    • Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation
    • Dusi S, Valletta L, Haack TB et al: Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation. Am J Hum Genet 2014; 94: 11-22.
    • (2014) Am J Hum Genet , vol.94 , pp. 11-22
    • Dusi, S.1    Valletta, L.2    Haack, T.B.3
  • 21
    • 84902074147 scopus 로고    scopus 로고
    • Molecular analysis, pathogenic mechanisms, and readthrough therapy on a large cohort of kabuki syndrome patients
    • Micale L, Augello B, Maffeo C et al: Molecular analysis, pathogenic mechanisms, and readthrough therapy on a large cohort of kabuki syndrome patients. Hum Mutat 2014; 35: 841-850.
    • (2014) Hum Mutat , vol.35 , pp. 841-850
    • Micale, L.1    Augello, B.2    Maffeo, C.3
  • 22
    • 84911435316 scopus 로고    scopus 로고
    • POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations
    • Di Costanzo S, Balasubramanian A, Pond HL et al: POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations. Hum Mol Genet 2014; 23: 5781-5792.
    • (2014) Hum Mol Genet , vol.23 , pp. 5781-5792
    • Di Costanzo, S.1    Balasubramanian, A.2    Pond, H.L.3
  • 23
    • 14644446021 scopus 로고    scopus 로고
    • Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells
    • Krause S, Hinderlich S, Amsili S et al: Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells. Exp Cell Res 2005; 304: 365-379.
    • (2005) Exp Cell Res , vol.304 , pp. 365-379
    • Krause, S.1    Hinderlich, S.2    Amsili, S.3
  • 24
    • 32944459691 scopus 로고    scopus 로고
    • Adenovirus vectors based on human adenovirus type 19a have high potential for human muscle-directed gene therapy
    • Thirion C, Lochmüller H, Ruzsics Z: Adenovirus vectors based on human adenovirus type 19a have high potential for human muscle-directed gene therapy. Hum Gene Ther 2006; 17: 193-205.
    • (2006) Hum Gene Ther , vol.17 , pp. 193-205
    • Thirion, C.1    Lochmüller, H.2    Ruzsics, Z.3
  • 25
    • 34047117380 scopus 로고    scopus 로고
    • The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy
    • Janiesch PC, Kim J, Mouysset J et al: The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy. Nat Cell Biol 2007; 9: 379-390.
    • (2007) Nat Cell Biol , vol.9 , pp. 379-390
    • Janiesch, P.C.1    Kim, J.2    Mouysset, J.3
  • 26
    • 64549089612 scopus 로고    scopus 로고
    • In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes
    • Bulst S, Abicht A, Holinski-Feder E et al: In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes. Hum Mol Genet 2009; 18: 1590-1599.
    • (2009) Hum Mol Genet , vol.18 , pp. 1590-1599
    • Bulst, S.1    Abicht, A.2    Holinski-Feder, E.3
  • 27
    • 77949269532 scopus 로고    scopus 로고
    • Muscle-derived Duchenne muscular dystrophy fibroblasts show altered production of extracellular matrix components
    • Zanotti S, Gibertini S, Mora M: Muscle-derived Duchenne muscular dystrophy fibroblasts show altered production of extracellular matrix components. Cell Tissue Res 2010; 339: 397-410.
    • (2010) Cell Tissue Res , vol.339 , pp. 397-410
    • Zanotti, S.1    Gibertini, S.2    Mora, M.3
  • 28
    • 79251595304 scopus 로고    scopus 로고
    • The human neurotrophin receptor p75NTR defines differentiation-oriented skeletal muscle precursor cells: Implications for muscle regeneration
    • Colombo E, Romaggi S, Medico E et al: The human neurotrophin receptor p75NTR defines differentiation-oriented skeletal muscle precursor cells: implications for muscle regeneration. J Neuropathol Exp Neurol 2011; 70: 133-142.
    • (2011) J Neuropathol Exp Neurol , vol.70 , pp. 133-142
    • Colombo, E.1    Romaggi, S.2    Medico, E.3
  • 29
    • 79951517541 scopus 로고    scopus 로고
    • Two new protocols to enhance the production and isolation of human induced pluripotent stem cell lines
    • Dick E, Matsa E, Bispham J et al: Two new protocols to enhance the production and isolation of human induced pluripotent stem cell lines. Stem Cell Res 2011; 6: 158-167.
    • (2011) Stem Cell Res , vol.6 , pp. 158-167
    • Dick, E.1    Matsa, E.2    Bispham, J.3
  • 30
    • 84865729644 scopus 로고    scopus 로고
    • Skin fibroblasts from pantothenate kinase-associate neurodegeneration patients show altered cellular oxidative status and have defective iron-handling properties
    • Campanella A, Privitera D, Guaraldo M et al: Skin fibroblasts from pantothenate kinase-associate neurodegeneration patients show altered cellular oxidative status and have defective iron-handling properties. Hum Mol Genet 2012; 21: 4049-4059.
    • (2012) Hum Mol Genet , vol.21 , pp. 4049-4059
    • Campanella, A.1    Privitera, D.2    Guaraldo, M.3
  • 31
    • 84863185444 scopus 로고    scopus 로고
    • Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy
    • Tedesco FS, Gerli MF, Perani L et al: Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy. Sci Transl Med 2012; 4: 140ra89.
    • (2012) Sci Transl Med , vol.4 , pp. 140-189
    • Tedesco, F.S.1    Gerli, M.F.2    Perani, L.3
  • 32
    • 84887510121 scopus 로고    scopus 로고
    • Mitochondrial DNA deletions in muscle satellite cells: Implications for therapies
    • Spendiff S, Reza M, Murphy JL et al: Mitochondrial DNA deletions in muscle satellite cells: implications for therapies. Hum Mol Genet 2013; 22: 4739-4747.
    • (2013) Hum Mol Genet , vol.22 , pp. 4739-4747
    • Spendiff, S.1    Reza, M.2    Murphy, J.L.3
  • 33
    • 84880647483 scopus 로고    scopus 로고
    • Flow cytometry for the analysis of dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathies
    • Stevens E, Torelli S, Feng L et al: Flow cytometry for the analysis of dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathies. PLoS One 2013; 8: e68958.
    • (2013) PLoS One , vol.8 , pp. e68958
    • Stevens, E.1    Torelli, S.2    Feng, L.3
  • 34
    • 84921411214 scopus 로고    scopus 로고
    • GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells
    • Livide G, Patriarchi T, Amenduni M et al: GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells. Eur J Hum Genet 2015; 23: 195-201.
    • (2015) Eur J Hum Genet , vol.23 , pp. 195-201
    • Livide, G.1    Patriarchi, T.2    Amenduni, M.3
  • 35
    • 33644522383 scopus 로고    scopus 로고
    • Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1
    • Gabellini D, D'Antona G, Moggio M et al: Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature 2006; 439: 973-977.
    • (2006) Nature , vol.439 , pp. 973-977
    • Gabellini, D.1    D'Antona, G.2    Moggio, M.3
  • 36
    • 36749019110 scopus 로고    scopus 로고
    • Distinctive patterns of microRNA expression in primary muscular disorders
    • USA
    • Eisenberg I, Eran A, Nishino I et al: Distinctive patterns of microRNA expression in primary muscular disorders. Proc Natl Acad Sci USA 2007; 104: 17016-17021.
    • (2007) Proc Natl Acad Sci , vol.104 , pp. 17016-17021
    • Eisenberg, I.1    Eran, A.2    Nishino, I.3
  • 37
    • 38949205725 scopus 로고    scopus 로고
    • Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients
    • Guglieri M, Magri F, D'Angelo MG et al: Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients. Hum Mutat 2008; 29: 258-266.
    • (2008) Hum Mutat , vol.29 , pp. 258-266
    • Guglieri, M.1    Magri, F.2    D'Angelo, M.G.3
  • 38
    • 79958853163 scopus 로고    scopus 로고
    • Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele
    • Meznaric M, Gonzalez-Quereda L, Gallardo E et al: Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele. Eur J Neurol 2011; 18: 1021-1023.
    • (2011) Eur J Neurol , vol.18 , pp. 1021-1023
    • Meznaric, M.1    Gonzalez-Quereda, L.2    Gallardo, E.3
  • 39
    • 80054880080 scopus 로고    scopus 로고
    • Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
    • Mutsaers CA, Wishart TM, Lamont DJ et al: Reversible molecular pathology of skeletal muscle in spinal muscular atrophy. Hum Mol Genet 2011; 20: 4334-4344.
    • (2011) Hum Mol Genet , vol.20 , pp. 4334-4344
    • Mutsaers, C.A.1    Wishart, T.M.2    Lamont, D.J.3
  • 41
    • 84874649008 scopus 로고    scopus 로고
    • Atrophy, fibrosis, and increased PAX7-positive cells in pharyngeal muscles of oculopharyngeal muscular dystrophy patients
    • Gidaro T, Negroni E, Perié S et al: Atrophy, fibrosis, and increased PAX7-positive cells in pharyngeal muscles of oculopharyngeal muscular dystrophy patients. J Neuropathol Exp Neurol 2013; 72: 234-243.
    • (2013) J Neuropathol Exp Neurol , vol.72 , pp. 234-243
    • Gidaro, T.1    Negroni, E.2    Perié, S.3
  • 42
    • 84896708393 scopus 로고    scopus 로고
    • Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies
    • Kalko SG, Paco S, Jou C et al: Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies. BMC Genomics 2014; 15: 91.
    • (2014) BMC Genomics , vol.15 , pp. 91
    • Kalko, S.G.1    Paco, S.2    Jou, C.3
  • 43
    • 84903740009 scopus 로고    scopus 로고
    • Affinity proteomics within rare diseases: A BIO-NMD study for blood biomarkers of muscular dystrophies
    • Ayoglu B, Chaouch A, Lochmüller H et al: Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies. EMBO Mol Med 2014; 6: 918-936.
    • (2014) EMBO Mol Med , vol.6 , pp. 918-936
    • Ayoglu, B.1    Chaouch, A.2    Lochmüller, H.3
  • 44
    • 85006186594 scopus 로고    scopus 로고
    • Quantifying the use of bioresources for promoting their sharing in scientific research
    • Mabile L, Dalgleish R, Thorisson GA et al: Quantifying the use of bioresources for promoting their sharing in scientific research. Gigascience 2013; 2: 7.
    • (2013) Gigascience , vol.2 , pp. 7
    • Mabile, L.1    Dalgleish, R.2    Thorisson, G.A.3
  • 45
    • 84971459735 scopus 로고    scopus 로고
    • Cell Line and DNA Biobank from patients affected by genetic diseases
    • Filocamo M, Mazzotti R, Corsolini F et al: Cell Line and DNA Biobank from patients affected by genetic diseases. Open J Bioresources 2014; 1: e2.
    • (2014) Open J Bioresources , vol.1 , pp. e2
    • Filocamo, M.1    Mazzotti, R.2    Corsolini, F.3
  • 46
    • 84879841885 scopus 로고    scopus 로고
    • International guidelines on biobank research leave researchers in ambiguity: Why is this so
    • Forsberg JS, Hansson MG, Evers K: International guidelines on biobank research leave researchers in ambiguity: why is this so? Eur J Epidemio 2013; 28: 449-451.
    • (2013) Eur J Epidemio , vol.28 , pp. 449-451
    • Forsberg, J.S.1    Hansson, M.G.2    Evers, K.3
  • 47
    • 84859566974 scopus 로고    scopus 로고
    • Managing incidental findings and research results in genomic research involving biobanks and archived data sets
    • Wolf SM, Crock BN, Van Ness B et al: Managing incidental findings and research results in genomic research involving biobanks and archived data sets. Genet Med 2012; 14: 361-384.
    • (2012) Genet Med , vol.14 , pp. 361-384
    • Wolf, S.M.1    Crock, B.N.2    Van Ness, B.3
  • 48
    • 84896542722 scopus 로고    scopus 로고
    • Incidental findings: The time is not yet ripe for a policy for biobanks
    • Viberg J, Hansson MG, Langenskiöld S, Segerdahl P: Incidental findings: the time is not yet ripe for a policy for biobanks. Eur J Hum Genet 2014; 22: 437-441.
    • (2014) Eur J Hum Genet , vol.22 , pp. 437-441
    • Viberg, J.1    Hansson, M.G.2    Langenskiöld, S.3    Segerdahl, P.4
  • 49
    • 84929288545 scopus 로고    scopus 로고
    • International Charter of principles for sharing bio-specimens and data
    • Mascalzoni D, Dove ES, Rubinstein Y et al: International Charter of principles for sharing bio-specimens and data. Eur J Hum Genet 2015; 23: 721-728.
    • (2015) Eur J Hum Genet , vol.23 , pp. 721-728
    • Mascalzoni, D.1    Dove, E.S.2    Rubinstein, Y.3
  • 50
    • 84882953314 scopus 로고    scopus 로고
    • A solidarity-based approach to the governance of research biobanks
    • Prainsack B, Buyx A: A solidarity-based approach to the governance of research biobanks. Med Law Rev 2013; 21: 71-91.
    • (2013) Med Law Rev , vol.21 , pp. 71-91
    • Prainsack, B.1    Buyx, A.2
  • 51
    • 84905859770 scopus 로고    scopus 로고
    • RD-Connect: An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research
    • Thompson R, Johnston L, Taruscio D et al: RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. J Gen Intern Med 2014; 29(Suppl 3): S780-S787.
    • (2014) J Gen Intern Med , vol.29 , pp. S780-S787
    • Thompson, R.1    Johnston, L.2    Taruscio, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.