A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female

被引：14

作者：

Lin, GS

Glass, JD

Shumas, S

Scherer, SS

Fischbeck, KH

机构：

[1] NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA

[2] Univ Penn, Med Ctr, Dept Neurol, Philadelphia, PA 19104 USA

[3] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA

来源：

CHARCOT-MARIE-TOOTH DISORDERS | 1999年 / 883卷

关键词：

D O I：

10.1111/j.1749-6632.1999.tb08616.x

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

[No abstract available]

引用

页码：481 / 484

页数：4

共 8 条

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