Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR):: findings from over 7000 newborns from 16 areas world wide

被引:384
作者
Wilcken, B
Bamforth, F
Li, Z
Zhu, H
Ritvanen, A
Redlund, M
Stoll, C
Alembik, Y
Dott, B
Czeizel, AE
Gelman-Kohan, Z
Scarano, G
Bianca, S
Ettore, G
Tenconi, R
Bellato, S
Scala, I
Mutchinick, OM
López, MA
de Walle, H
Hofstra, R
Joutchenko, L
Kavteladze, L
Bermejo, E
Martínez-Frías, ML
Gallagher, M
Erickson, JD
Vollset, SE
Mastroiacovo, P
Andria, G
Botto, LD
机构
[1] Childrens Hosp Westmead, Sydney, NSW, Australia
[2] Univ Alberta, Edmonton, AB, Canada
[3] Peking Univ, Natl Ctr Maternal & Infant Hlth, Beijing 100871, Peoples R China
[4] Natl Res & Dev Ctr Welf & Hlth, STAKES, Helsinki, Finland
[5] Univ Helsinki, Cent Hosp, Dept Paediat, FIN-00014 Helsinki, Finland
[6] Univ Strasbourg, Strasbourg, France
[7] Fdn Community Control Hereditary Dis, Budapest, Hungary
[8] Kaplan Med Ctr, Rehovot, Israel
[9] AO G Rummo, Div Med Genet, Benevento, Italy
[10] Birth Defects Registry, Campania, Italy
[11] Sicily Congenital Malformat Registry, Sicily, Italy
[12] Univ Padua, Dept Paediat, Veneto, Italy
[13] Arzignano Hosp, Paediat Unit, Vicenza, Veneto, Italy
[14] Univ Naples Federico II, Naples, Italy
[15] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Genet, RYVEMCE, Mexico City, DF, Mexico
[16] Univ Groningen, NL-9700 AB Groningen, Netherlands
[17] Moscow Birth Defects Registry, Moscow, Russia
[18] ECEMC, Madrid, Spain
[19] Inst Salud Carlos III, Madrid, Spain
[20] Univ Complutense, E-28040 Madrid, Spain
[21] CDCP, Natl Ctr Environm Hlth, Atlanta, GA USA
[22] CDCP, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA 30341 USA
[23] Univ Bergen, Bergen, Norway
[24] Int Ctr Birth Defects, Rome, Italy
关键词
D O I
10.1136/jmg.40.8.619
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:619 / 625
页数:7
相关论文
共 31 条
[11]  
James SJ, 1999, AM J CLIN NUTR, V70, P495
[12]  
KANG SS, 1991, AM J HUM GENET, V48, P536
[13]  
Khoury MJ, 2000, AM J EPIDEMIOL, V151, P2
[14]  
Mills JL, 1999, AM J MED GENET, V86, P71, DOI 10.1002/(SICI)1096-8628(19990903)86:1<71::AID-AJMG14>3.3.CO
[15]  
2-P
[16]  
Moore CA, 1997, AM J MED GENET, V73, P113
[17]   A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians [J].
Mukherjee, M ;
Joshi, S ;
Bagadi, S ;
Dalvi, M ;
Rao, A ;
Shetty, KR .
CLINICAL GENETICS, 2002, 61 (02) :155-159
[18]   High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico:: A country with a very high prevalence of neural tube defects [J].
Mutchinick, OM ;
López, MA ;
Luna, L ;
Waxman, J ;
Babinsky, VE .
MOLECULAR GENETICS AND METABOLISM, 1999, 68 (04) :461-467
[19]   MTRR and MTHFR polymorphism: Link to Down syndrome? [J].
O'Leary, VB ;
Parle-McDermott, A ;
Molloy, AM ;
Kirke, PN ;
Johnson, Z ;
Conley, M ;
Scott, JM ;
Mills, JL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 107 (02) :151-155
[20]   Methylenetetrahydrofolate reductase 677 C→T polymorphism, plasma folate, vitamin B12 concentrations, and risk of preeclampsia among black African women from Zimbabwe [J].
Rajkovic, A ;
Mahomed, K ;
Rozen, R ;
Malinow, MR ;
King, IB ;
Williams, MA .
MOLECULAR GENETICS AND METABOLISM, 2000, 69 (01) :33-39