메뉴 건너뛰기




Volumn 1, Issue 2, 2015, Pages 214-221

Germline TP53 mutations in patients with early-onset colorectal cancer in the Colon Cancer Family Registry

(14)  Yurgelun, Matthew B a,b   Masciari, Serena a   Joshi, Victoria A c   Mercado, Rowena C a   Lindor, Noralane M d   Gallinger, Steven e   Hopper, John L f   Jenkins, Mark A f   Buchanan, Daniel D f   Newcomb, Polly A g   Potter, John D g,h,i   Haile, Robert W j   Kucherlapati, Raju b,c   Syngal, Sapna a,b,k  


Author keywords

[No Author keywords available]

Indexed keywords

DNA GLYCOSYLASE MUTY; DNA GLYCOSYLTRANSFERASE; PROTEIN P53; TP53 PROTEIN, HUMAN; TUMOR MARKER;

EID: 84994508622     PISSN: 23742437     EISSN: 23742445     Source Type: Journal    
DOI: 10.1001/jamaoncol.2015.0197     Document Type: Article
Times cited : (71)

References (49)
  • 1
    • 84897575984 scopus 로고    scopus 로고
    • The increasing incidence of young-onset colorectal cancer: A call to action
    • Ahnen DJ, Wade SW, Jones WF, et al. The increasing incidence of young-onset colorectal cancer: a call to action. Mayo Clin Proc. 2014;89(2):216-224.
    • (2014) Mayo Clin Proc. , vol.89 , Issue.2 , pp. 216-224
    • Ahnen, D.J.1    Wade, S.W.2    Jones, W.F.3
  • 2
    • 84864542171 scopus 로고    scopus 로고
    • Clinicopathologic and molecular features of sporadic early-onset colorectal adenocarcinoma: An adenocarcinoma with frequent signet ring cell differentiation, rectal and sigmoid involvement, and adverse morphologic features
    • Chang DT, Pai RK, Rybicki LA, et al. Clinicopathologic and molecular features of sporadic early-onset colorectal adenocarcinoma: an adenocarcinoma with frequent signet ring cell differentiation, rectal and sigmoid involvement, and adverse morphologic features. Mod Pathol. 2012;25(8):1128-1139.
    • (2012) Mod Pathol. , vol.25 , Issue.8 , pp. 1128-1139
    • Chang, D.T.1    Pai, R.K.2    Rybicki, L.A.3
  • 3
    • 79957469844 scopus 로고    scopus 로고
    • Prevalence of alterations in DNA mismatch repair genes in patients with young-onset colorectal cancer
    • Limburg PJ, Harmsen WS, Chen HH, et al. Prevalence of alterations in DNA mismatch repair genes in patients with young-onset colorectal cancer. Clin Gastroenterol Hepatol. 2011;9(6):497-502.
    • (2011) Clin Gastroenterol Hepatol. , vol.9 , Issue.6 , pp. 497-502
    • Limburg, P.J.1    Harmsen, W.S.2    Chen, H.H.3
  • 4
    • 78349250964 scopus 로고    scopus 로고
    • MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer
    • Giráldez MD, Balaguer F, Bujanda L, et al. MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer. Clin Cancer Res.2010;16(22):5402-5413.
    • (2010) Clin Cancer Res. , vol.16 , Issue.22 , pp. 5402-5413
    • Giráldez, M.D.1    Balaguer, F.2    Bujanda, L.3
  • 5
    • 84902544333 scopus 로고    scopus 로고
    • Familial colorectal cancer, beyond Lynch syndrome
    • Stoffel EM, Kastrinos F. Familial colorectal cancer, beyond Lynch syndrome. Clin Gastroenterol Hepatol. 2014;12(7):1059-1068.
    • (2014) Clin Gastroenterol Hepatol. , vol.12 , Issue.7 , pp. 1059-1068
    • Stoffel, E.M.1    Kastrinos, F.2
  • 6
    • 30044447282 scopus 로고    scopus 로고
    • Prevalence of early onset colorectal cancer in 397 patients with classic Li-Fraumeni syndrome
    • Wong P, Verselis SJ, Garber JE, et al. Prevalence of early onset colorectal cancer in 397 patients with classic Li-Fraumeni syndrome. Gastroenterology. 2006;130(1):73-79.
    • (2006) Gastroenterology , vol.130 , Issue.1 , pp. 73-79
    • Wong, P.1    Verselis, S.J.2    Garber, J.E.3
  • 7
    • 0014587529 scopus 로고
    • Soft-tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome?
    • Li FP, Fraumeni JF Jr. Soft-tissue sarcomas, breast cancer, and other neoplasms: a familial syndrome? Ann Intern Med. 1969;71(4):747-752.
    • (1969) Ann Intern Med. , vol.71 , Issue.4 , pp. 747-752
    • Li, F.P.1    Fraumeni, J.F.2
  • 8
    • 0023715595 scopus 로고
    • A cancer family syndrome in twenty-four kindreds
    • Li FP, Fraumeni JF Jr, Mulvihill JJ, et al. A cancer family syndrome in twenty-four kindreds. Cancer Res. 1988;48(18):5358-5362.
    • (1988) Cancer Res. , vol.48 , Issue.18 , pp. 5358-5362
    • Li, F.P.1    Fraumeni, J.F.2    Mulvihill, J.J.3
  • 10
    • 80053022230 scopus 로고    scopus 로고
    • Li-fraumeni syndrome
    • Malkin D. Li-fraumeni syndrome. Genes Cancer. 2011;2(4):475-484.
    • (2011) Genes Cancer , vol.2 , Issue.4 , pp. 475-484
    • Malkin, D.1
  • 11
    • 62449249871 scopus 로고    scopus 로고
    • Beyond Li Fraumeni syndrome: Clinical characteristics of families with p53 germline mutations
    • Gonzalez KD, Noltner KA, Buzin CH, et al. Beyond Li Fraumeni syndrome: clinical characteristics of families with p53 germline mutations. J Clin Oncol. 2009;27(8):1250-1256.
    • (2009) J Clin Oncol. , vol.27 , Issue.8 , pp. 1250-1256
    • Gonzalez, K.D.1    Noltner, K.A.2    Buzin, C.H.3
  • 12
    • 79960845375 scopus 로고    scopus 로고
    • Gastric cancer in individuals with Li-Fraumeni syndrome
    • Masciari S, Dewanwala A, Stoffel EM, et al. Gastric cancer in individuals with Li-Fraumeni syndrome. Genet Med. 2011;13(7):651-657.
    • (2011) Genet Med. , vol.13 , Issue.7 , pp. 651-657
    • Masciari, S.1    Dewanwala, A.2    Stoffel, E.M.3
  • 13
    • 0035133356 scopus 로고    scopus 로고
    • Sensitivity and predictive value of criteria for p53 germline mutation screening
    • Chompret A, Abel A, Stoppa-Lyonnet D, et al. Sensitivity and predictive value of criteria for p53 germline mutation screening. J Med Genet. 2001;38(1):43-47.
    • (2001) J Med Genet. , vol.38 , Issue.1 , pp. 43-47
    • Chompret, A.1    Abel, A.2    Stoppa-Lyonnet, D.3
  • 14
    • 70349320378 scopus 로고    scopus 로고
    • 2009 Version of the Chompret criteria for Li Fraumeni syndrome
    • Tinat J, Bougeard G, Baert-Desurmont S, et al. 2009 version of the Chompret criteria for Li Fraumeni syndrome. J Clin Oncol. 2009;27(26):e108-e109.
    • (2009) J Clin Oncol. , vol.27 , Issue.26 , pp. e108-e109
    • Tinat, J.1    Bougeard, G.2    Baert-Desurmont, S.3
  • 15
    • 84876071726 scopus 로고    scopus 로고
    • Multiplex genetic testing for cancer susceptibility: Out on the high wire without a net?
    • Domchek SM, Bradbury A, Garber JE, Offit K, Robson ME. Multiplex genetic testing for cancer susceptibility: out on the high wire without a net? J Clin Oncol. 2013;31(10):1267-1270.
    • (2013) J Clin Oncol. , vol.31 , Issue.10 , pp. 1267-1270
    • Domchek, S.M.1    Bradbury, A.2    Garber, J.E.3    Offit, K.4    Robson, M.E.5
  • 16
    • 38849170356 scopus 로고    scopus 로고
    • Colon Cancer Family Registry: An international resource for studies of the genetic epidemiology of colon cancer
    • Newcomb PA, Baron J, Cotterchio M, et al; Colon Cancer Family Registry. Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. Cancer Epidemiol Biomarkers Prev. 2007;16(11):2331-2343.
    • (2007) Cancer Epidemiol Biomarkers Prev. , vol.16 , Issue.11 , pp. 2331-2343
    • Newcomb, P.A.1    Baron, J.2    Cotterchio, M.3
  • 17
    • 34248379012 scopus 로고    scopus 로고
    • Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: Lessons from recent developments in the IARC TP53 database
    • Petitjean A, Mathe E, Kato S, et al. Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database. Hum Mutat. 2007;28(6):622-629.
    • (2007) Hum Mutat. , vol.28 , Issue.6 , pp. 622-629
    • Petitjean, A.1    Mathe, E.2    Kato, S.3
  • 18
    • 62949228316 scopus 로고    scopus 로고
    • Germline MutY human homologue mutations and colorectal cancer: A multisite case-control study
    • Cleary SP, Cotterchio M, Jenkins MA, et al. Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study. Gastroenterology. 2009;136(4):1251-1260.
    • (2009) Gastroenterology , vol.136 , Issue.4 , pp. 1251-1260
    • Cleary, S.P.1    Cotterchio, M.2    Jenkins, M.A.3
  • 19
    • 0035026704 scopus 로고    scopus 로고
    • Predicting deleterious amino acid substitutions
    • Ng PC, Henikoff S. Predicting deleterious amino acid substitutions. Genome Res. 2001;11(5):863-874.
    • (2001) Genome Res. , vol.11 , Issue.5 , pp. 863-874
    • Ng, P.C.1    Henikoff, S.2
  • 20
    • 77951640946 scopus 로고    scopus 로고
    • A method and server for predicting damaging missense mutations
    • Adzhubei IA, Schmidt S, Peshkin L, et al. A method and server for predicting damaging missense mutations. Nat Methods. 2010;7(4):248-249.
    • (2010) Nat Methods. , vol.7 , Issue.4 , pp. 248-249
    • Adzhubei, I.A.1    Schmidt, S.2    Peshkin, L.3
  • 21
    • 85010217212 scopus 로고    scopus 로고
    • Accessed May 2, 2014
    • Exome Variant Server NGESPE, Seattle WA. http://evs.gs.washington.edu/EVS/. Accessed May 2, 2014.
  • 22
    • 12944260522 scopus 로고    scopus 로고
    • Successful treatment of an unresectable choroid plexus carcinoma in a patient with Li-Fraumeni syndrome
    • Dickens DS, Dothage JA, Heideman RL, Ballard ET, Jubinsky PT. Successful treatment of an unresectable choroid plexus carcinoma in a patient with Li-Fraumeni syndrome. J Pediatr Hematol Oncol. 2005;27(1):46-49.
    • (2005) J Pediatr Hematol Oncol. , vol.27 , Issue.1 , pp. 46-49
    • Dickens, D.S.1    Dothage, J.A.2    Heideman, R.L.3    Ballard, E.T.4    Jubinsky, P.T.5
  • 23
    • 33847691863 scopus 로고    scopus 로고
    • Younger age of cancer initiation is associated with shorter telomere length in Li-Fraumeni syndrome
    • Tabori U, Nanda S, Druker H, Lees J, Malkin D. Younger age of cancer initiation is associated with shorter telomere length in Li-Fraumeni syndrome. Cancer Res. 2007;67(4):1415-1418.
    • (2007) Cancer Res. , vol.67 , Issue.4 , pp. 1415-1418
    • Tabori, U.1    Nanda, S.2    Druker, H.3    Lees, J.4    Malkin, D.5
  • 24
    • 0033365202 scopus 로고    scopus 로고
    • Are there low-penetrance TP53 alleles? Evidence from childhood adrenocortical tumors
    • Varley JM, McGown G, Thorncroft M, et al. Are there low-penetrance TP53 alleles? evidence from childhood adrenocortical tumors. Am J Hum Genet. 1999;65(4):995-1006.
    • (1999) Am J Hum Genet. , vol.65 , Issue.4 , pp. 995-1006
    • Varley, J.M.1    McGown, G.2    Thorncroft, M.3
  • 26
    • 0033016982 scopus 로고    scopus 로고
    • High frequency of TP53 mutations in juvenile pilocytic astrocytomas indicates role of TP53 in the development of these tumors
    • Hayes VM, Dirven CM, Dam A, et al. High frequency of TP53 mutations in juvenile pilocytic astrocytomas indicates role of TP53 in the development of these tumors. Brain Pathol. 1999;9(3):463-467.
    • (1999) Brain Pathol. , vol.9 , Issue.3 , pp. 463-467
    • Hayes, V.M.1    Dirven, C.M.2    Dam, A.3
  • 27
    • 70449519172 scopus 로고    scopus 로고
    • TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset
    • Pinto C, Veiga I, Pinheiro M, et al. TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset. Fam Cancer. 2009;8(4):383-390.
    • (2009) Fam Cancer. , vol.8 , Issue.4 , pp. 383-390
    • Pinto, C.1    Veiga, I.2    Pinheiro, M.3
  • 28
    • 41149160304 scopus 로고    scopus 로고
    • Germline TP53 mutations in BRCA1 and BRCA2 mutation-negative French Canadian breast cancer families
    • Arcand SL, Maugard CM, Ghadirian P, et al. Germline TP53 mutations in BRCA1 and BRCA2 mutation-negative French Canadian breast cancer families. Breast Cancer Res Treat. 2008;108(3):399-408.
    • (2008) Breast Cancer Res Treat , vol.108 , Issue.3 , pp. 399-408
    • Arcand, S.L.1    Maugard, C.M.2    Ghadirian, P.3
  • 29
    • 0033536239 scopus 로고    scopus 로고
    • p53 compound heterozygosity in a severely affected child with Li-Fraumeni syndrome
    • Quesnel S, Verselis S, Portwine C, et al. p53 compound heterozygosity in a severely affected child with Li-Fraumeni syndrome. Oncogene. 1999;18(27):3970-3978.
    • (1999) Oncogene , vol.18 , Issue.27 , pp. 3970-3978
    • Quesnel, S.1    Verselis, S.2    Portwine, C.3
  • 30
    • 33846581859 scopus 로고    scopus 로고
    • Germline mutations of TP53 and BRCA2 genes in breast cancer/sarcoma families
    • Manoukian S, Peissel B, Pensotti V, et al. Germline mutations of TP53 and BRCA2 genes in breast cancer/sarcoma families. Eur J Cancer.2007;43(3):601-606.
    • (2007) Eur J Cancer. , vol.43 , Issue.3 , pp. 601-606
    • Manoukian, S.1    Peissel, B.2    Pensotti, V.3
  • 31
    • 19444376902 scopus 로고    scopus 로고
    • Germline mutations of the E-cadherin (CDH1) and TP53 genes, rather than of RUNX3 and HPP1, contribute to genetic predisposition in German gastric cancer patients
    • Keller G, Vogelsang H, Becker I, et al. Germline mutations of the E-cadherin (CDH1) and TP53 genes, rather than of RUNX3 and HPP1, contribute to genetic predisposition in German gastric cancer patients. J Med Genet.2004;41(6):e89.
    • (2004) J Med Genet. , vol.41 , Issue.6 , pp. e89
    • Keller, G.1    Vogelsang, H.2    Becker, I.3
  • 32
    • 84856770553 scopus 로고    scopus 로고
    • Early onset HER2-positive breast cancer is associated with germline TP53 mutations
    • Melhem-Bertrandt A, Bojadzieva J, Ready KJ, et al. Early onset HER2-positive breast cancer is associated with germline TP53 mutations. Cancer. 2012;118(4):908-913.
    • (2012) Cancer , vol.118 , Issue.4 , pp. 908-913
    • Melhem-Bertrandt, A.1    Bojadzieva, J.2    Ready, K.J.3
  • 33
    • 84880660114 scopus 로고    scopus 로고
    • High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort
    • Mitchell G, Ballinger ML, Wong S, et al; International Sarcoma Kindred Study. High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort. PLoS One. 2013;8(7):e69026.
    • (2013) PLoS One , vol.8 , Issue.7
    • Mitchell, G.1    Ballinger, M.L.2    Wong, S.3
  • 34
    • 79958750215 scopus 로고    scopus 로고
    • A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: Analysis of 1287 diagnostic and 1148 follow-up CLL samples
    • Pekova S, Mazal O, Cmejla R, et al. A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: analysis of 1287 diagnostic and 1148 follow-up CLL samples. Leuk Res. 2011;35(7):889-898.
    • (2011) Leuk Res. , vol.35 , Issue.7 , pp. 889-898
    • Pekova, S.1    Mazal, O.2    Cmejla, R.3
  • 35
    • 0028958465 scopus 로고
    • Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma
    • Diller L, Sexsmith E, Gottlieb A, Li FP, Malkin D. Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma. J Clin Invest. 1995;95(4):1606-1611.
    • (1995) J Clin Invest. , vol.95 , Issue.4 , pp. 1606-1611
    • Diller, L.1    Sexsmith, E.2    Gottlieb, A.3    Li, F.P.4    Malkin, D.5
  • 37
    • 0033167278 scopus 로고    scopus 로고
    • Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2
    • Huusko P, Castrén K, Launonen V, et al. Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2. Cancer Genet Cytogenet. 1999;112(1):9-14.
    • (1999) Cancer Genet Cytogenet. , vol.112 , Issue.1 , pp. 9-14
    • Huusko, P.1    Castrén, K.2    Launonen, V.3
  • 38
    • 34547447094 scopus 로고    scopus 로고
    • Two TP53 germline mutations in a classical Li-Fraumeni syndrome family
    • van Hest LP, Ruijs MW, Wagner A, et al. Two TP53 germline mutations in a classical Li-Fraumeni syndrome family. Fam Cancer. 2007;6(3):311-316.
    • (2007) Fam Cancer. , vol.6 , Issue.3 , pp. 311-316
    • Van Hest, L.P.1    Ruijs, M.W.2    Wagner, A.3
  • 39
    • 77955019941 scopus 로고    scopus 로고
    • Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis
    • Jasperson KW, Vu TM, Schwab AL, et al. Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis. Fam Cancer. 2010;9(2):99-107.
    • (2010) Fam Cancer , vol.9 , Issue.2 , pp. 99-107
    • Jasperson, K.W.1    Vu, T.M.2    Schwab, A.L.3
  • 40
    • 77953734977 scopus 로고    scopus 로고
    • Population-based estimate of the contribution of TP53 mutations to subgroups of early-onset breast cancer: Australian Breast Cancer Family Study
    • Mouchawar J, Korch C, Byers T, et al. Population-based estimate of the contribution of TP53 mutations to subgroups of early-onset breast cancer: Australian Breast Cancer Family Study. Cancer Res. 2010;70(12):4795-4800.
    • (2010) Cancer Res. , vol.70 , Issue.12 , pp. 4795-4800
    • Mouchawar, J.1    Korch, C.2    Byers, T.3
  • 41
    • 33646394043 scopus 로고    scopus 로고
    • BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives
    • Lalloo F, Varley J, Moran A, et al. BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives. Eur J Cancer. 2006;42(8):1143-1150.
    • (2006) Eur J Cancer. , vol.42 , Issue.8 , pp. 1143-1150
    • Lalloo, F.1    Varley, J.2    Moran, A.3
  • 43
    • 70349705753 scopus 로고    scopus 로고
    • High frequency of de novo mutations in Li-Fraumeni syndrome
    • Gonzalez KD, Buzin CH, Noltner KA, et al. High frequency of de novo mutations in Li-Fraumeni syndrome. J Med Genet. 2009;46(10):689-693.
    • (2009) J Med Genet. , vol.46 , Issue.10 , pp. 689-693
    • Gonzalez, K.D.1    Buzin, C.H.2    Noltner, K.A.3
  • 44
    • 50049112746 scopus 로고    scopus 로고
    • Molecular basis of the Li-Fraumeni syndrome: An update from the French LFS families
    • Bougeard G, Sesboüé R, Baert-Desurmont S, et al; French LFS Working Group. Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families. J Med Genet. 2008;45(8):535-538.
    • (2008) J Med Genet. , vol.45 , Issue.8 , pp. 535-538
    • Bougeard, G.1    Sesboüé, R.2    Baert-Desurmont, S.3
  • 45
    • 0142157701 scopus 로고    scopus 로고
    • Li-Fraumeni and related syndromes: Correlation between tumor type, family structure, and TP53 genotype
    • Olivier M, Goldgar DE, Sodha N, et al. Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype. Cancer Res. 2003;63(20):6643-6650.
    • (2003) Cancer Res. , vol.63 , Issue.20 , pp. 6643-6650
    • Olivier, M.1    Goldgar, D.E.2    Sodha, N.3
  • 46
    • 40949118501 scopus 로고    scopus 로고
    • F18-fluorodeoxyglucose-positron emission tomography/computed tomography screening in Li-Fraumeni syndrome
    • Masciari S, Van den Abbeele AD, Diller LR, et al. F18-fluorodeoxyglucose-positron emission tomography/computed tomography screening in Li-Fraumeni syndrome. JAMA. 2008;299(11):1315-1319.
    • (2008) JAMA , vol.299 , Issue.11 , pp. 1315-1319
    • Masciari, S.1    Van Den Abbeele, A.D.2    Diller, L.R.3
  • 47
    • 19144365420 scopus 로고    scopus 로고
    • Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16
    • Wijnen J, Khan PM, Vasen H, et al. Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16. Am J Hum Genet. 1996;58(2):300-307.
    • (1996) Am J Hum Genet. , vol.58 , Issue.2 , pp. 300-307
    • Wijnen, J.1    Khan, P.M.2    Vasen, H.3
  • 48
    • 84864506477 scopus 로고    scopus 로고
    • Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas
    • Grover S, Kastrinos F, Steyerberg EW, et al. Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas. JAMA. 2012;308(5):485-492.
    • (2012) JAMA , vol.308 , Issue.5 , pp. 485-492
    • Grover, S.1    Kastrinos, F.2    Steyerberg, E.W.3
  • 49
    • 84867499525 scopus 로고    scopus 로고
    • Identification of Lynch syndrome among patients with colorectal cancer
    • Moreira L, Balaguer F, Lindor N, et al; EPICOLON Consortium. Identification of Lynch syndrome among patients with colorectal cancer. JAMA. 2012;308(15):1555-1565.
    • (2012) JAMA , vol.308 , Issue.15 , pp. 1555-1565
    • Moreira, L.1    Balaguer, F.2    Lindor, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.