Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

被引:236
作者
Schneider, JA [1 ]
Rees, DC [1 ]
Liu, YT [1 ]
Clegg, JB [1 ]
机构
[1] John Radcliffe Hosp, Inst Mol Med, MRC, Mol Haematol Unit, Oxford OX3 9DS, England
关键词
D O I
10.1086/301836
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:1258 / 1260
页数:3
相关论文
共 15 条
[1]  
Chen J, 1996, CANCER RES, V56, P4862
[2]  
ENGBERSEN AMT, 1995, AM J HUM GENET, V56, P142
[3]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[4]   Global distribution of the CCR5 gene 32-basepair deletion [J].
Martinson, JJ ;
Chapman, NH ;
Rees, DC ;
Liu, YT ;
Clegg, JB .
NATURE GENETICS, 1997, 16 (01) :100-103
[5]   Global prevalence of putative haemochromatosis mutations [J].
MerryweatherClarke, AT ;
Pointon, JJ ;
Shearman, JD ;
Robson, KJH .
JOURNAL OF MEDICAL GENETICS, 1997, 34 (04) :275-278
[6]  
Murray CJL, 1996, Global Health Statistics
[7]   Methylenetetrahydrofolate reductase and neural tube defects [J].
Papapetrou, C ;
Lynch, SA ;
Burn, J ;
Edwards, YH .
LANCET, 1996, 348 (9019) :58-58
[8]   WORLD DISTRIBUTION OF FACTOR-V LEIDEN [J].
REES, DC ;
COX, M ;
CLEGG, JB .
LANCET, 1995, 346 (8983) :1133-1134
[10]  
SMITHELLS RW, 1980, LANCET, V1, P339