The molecular basis of glutamate formiminotransferase deficiency (vol 22, pg 67, 2003)

被引:0
作者
Hilton, JE
Christensen, KE
Watkins, D
Raby, BA
Renaud, Y
de la Luna, S
Estivill, X
MacKenzie, RE
Hudson, TJ
Rosenblatt, DS
机构
[1] McGill Univ, Div Med Genet, Ctr Hlth, Dept Med, Montreal, PQ H3A 1A1, Canada
[2] McGill Univ, Dept Biol, Montreal, PQ H3A 1B1, Canada
[3] McGill Univ, Dept Biochem, Montreal, PQ H3A 1B1, Canada
[4] McGill Univ, Ctr Hlth, Inst Res, Montreal Genome Ctr, Montreal, PQ, Canada
[5] Genom Regulat Ctr, Barcelona, Spain
[6] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[7] McGill Univ, Dept Med, Montreal, PQ, Canada
[8] McGill Univ, Dept Pediat, Montreal, PQ H3A 2T5, Canada
关键词
D O I
10.1002/humu.10281
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:416 / 416
页数:1
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[1]   The molecular basis of glutamate formiminotransferase deficiency [J].
Hilton, JE ;
Christensen, KE ;
Watkins, D ;
Raby, BA ;
Renaud, Y ;
de la Luna, S ;
Estivill, X ;
MacKenzie, RE ;
Hudson, TJ ;
Rosenblatt, DS .
HUMAN MUTATION, 2003, 22 (01) :67-73