A point mutation in Codon 3 of connexin-32 is associated with X-linked Charcot-Marie-Tooth neuropathy

被引：0
|
作者：
Gupta, S
Benstead, T
Neumann, P
Guernsey, D
机构：
[1] DALHOUSIE UNIV, FAC MED, DEPT PATHOL, DIV MOL PATHOL & MOL GENET, HALIFAX, NS B3H 4H7, CANADA
[2] DALHOUSIE UNIV, FAC MED, DEPT MED, DIV NEUROL, HALIFAX, NS B3H 4H7, CANADA
[3] DALHOUSIE UNIV, FAC MED, DEPT ANAT & NEUROBIOL, HALIFAX, NS B3H 4H7, CANADA
来源：
HUMAN MUTATION | 1996年 / 8卷 / 04期
关键词：
D O I：
10.1002/(SICI)1098-1004(1996)8:4<375::AID-HUMU14>3.0.CO;2-#
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：375 / 376
页数：2
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