THE WILSON DISEASE GENE - CLINICAL IMPLICATIONS

被引:0
作者
COX, DW
THOMAS, GR
ROBERTS, EA
WALSHE, JM
机构
[1] HOSP SICK CHILDREN,TORONTO M5G 1X8,ONTARIO,CANADA
[2] UNIV TORONTO,DEPT PAEDIAT,TORONTO M5S 1A1,ONTARIO,CANADA
[3] UNIV TORONTO,DEPT MOLEC & MED GENET,TORONTO M5S 1A1,ONTARIO,CANADA
[4] MIDDLESEX HOSP,LONDON W1,ENGLAND
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D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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页码:A267 / A267
页数:1
相关论文
共 2 条
[1]   THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J].
BULL, PC ;
THOMAS, GR ;
ROMMENS, JM ;
FORBES, JR ;
COX, DW .
NATURE GENETICS, 1993, 5 (04) :327-337
[2]  
THOMAS, 1994, AM J HUM GENET, V51, P74