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Volumn 36, Issue 8, 2015, Pages 2444.e1-2444.e4

EIF4G1 mutations do not cause Parkinson's disease

Author keywords

EIF4G1; Genetics; Mutation; Parkinson's disease

Indexed keywords

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; EIF4G1 GENE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MIDDLE AGED; MUTATIONAL ANALYSIS; PARKINSON DISEASE; PRIORITY JOURNAL; GENE FREQUENCY; GENETIC ASSOCIATION STUDY; GENETICS; MUTATION;

EID: 84952636767     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2015.04.017     Document Type: Article
Times cited : (22)

References (11)
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    • 84887233439 scopus 로고    scopus 로고
    • EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa
    • Blanckenberg J., Ntsapi C., Carr J.A., Bardien S. EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa. Neurobiol. Aging 2014, 35:445.e1-445.e3.
    • (2014) Neurobiol. Aging , vol.35 , pp. 445.e1-445.e3
    • Blanckenberg, J.1    Ntsapi, C.2    Carr, J.A.3    Bardien, S.4
  • 8
    • 84939599004 scopus 로고    scopus 로고
    • Largescale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
    • International Parkinson's Disease Genomics Consortium (IPDGC); Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI); 23andMe; GenePD; NeuroGenetics Research Consortium (NGRC); Hussman Institute of Human Genomics (HIHG); Ashkenazi Jewish Dataset Investigator; Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE); North American Brain Expression Consortium (NABEC); United Kingdom Brain Expression Consortium (UKBEC); Greek Parkinson's Disease Consortium; Alzheimer Genetic Analysis Group, Ikram M.A., Ioannidis J.P., Hadjigeorgiou G.M., Bis J.C., Martinez M., Perlmutter J.S., Goate A., Marder K., Fiske B., Sutherland M., Xiromerisiou G., Myers R.H., Clark L.N., Stefansson K., Hardy J.A., Heutink P., Chen H., Wood N.W., Houlden H., Payami H., Brice A., Scott W.K., Gasser T., Bertram L., Eriksson N., Foroud T., Singleton A.B.
    • Nalls, M.A., Pankratz, N., Lill, C.M., Do, C.B., Hernandez, D.G., Saad, M., DeStefano, A.L., Kara E., Bras J., Sharma M., Schulte C., Keller M.F., Arepalli S., Letson C., Edsall C., Stefansson H., Liu X., Pliner H., Lee J.H., Cheng R.; International Parkinson's Disease Genomics Consortium (IPDGC); Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI); 23andMe; GenePD; NeuroGenetics Research Consortium (NGRC); Hussman Institute of Human Genomics (HIHG); Ashkenazi Jewish Dataset Investigator; Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE); North American Brain Expression Consortium (NABEC); United Kingdom Brain Expression Consortium (UKBEC); Greek Parkinson's Disease Consortium; Alzheimer Genetic Analysis Group, Ikram M.A., Ioannidis J.P., Hadjigeorgiou G.M., Bis J.C., Martinez M., Perlmutter J.S., Goate A., Marder K., Fiske B., Sutherland M., Xiromerisiou G., Myers R.H., Clark L.N., Stefansson K., Hardy J.A., Heutink P., Chen H., Wood N.W., Houlden H., Payami H., Brice A., Scott W.K., Gasser T., Bertram L., Eriksson N., Foroud T., Singleton A.B., 2014. Largescale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat. Genet. 46, 989-993.
    • (2014) Nat. Genet. , vol.46 , pp. 989-993
    • Nalls, M.A.1    Pankratz, N.2    Lill, C.M.3    Do, C.B.4    Hernandez, D.G.5    Saad, M.6    DeStefano, A.L.7    Kara, E.8    Bras, J.9    Sharma, M.10    Schulte, C.11    Keller, M.F.12    Arepalli, S.13    Letson, C.14    Edsall, C.15    Stefansson, H.16    Liu, X.17    Pliner, H.18    Lee, J.H.19    Cheng, R.20    more..


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.