A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathy

被引：8

作者：

GuiraudChaumeil, C

Vincent, MC

Laporte, J

Fardeau, M

Samson, F

Mandel, JL

机构：

[1] UNIV STRASBOURG 1,IGBMC,INSERM,CNRS,F-67404 ILLKIRCH GRAFFENS,FRANCE

[2] CHRU,STRASBOURG,FRANCE

[3] FAC MED,LAB GENET MOL HUMAINE,STRASBOURG,FRANCE

[4] CNRS URA 1159,LE PLESSIS ROBINS,FRANCE

[5] INST MYOL,INSERM U153,PARIS,FRANCE

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 60卷 / 06期

关键词：

D O I：

10.1016/S0002-9297(07)64249-9

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1542 / 1544

页数：3

共 8 条

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Dahl, N .

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Dahl, N .

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[8] THE MYOTUBULAR MYOPATHIES - DIFFERENTIAL-DIAGNOSIS OF THE X-LINKED RECESSIVE, AUTOSOMAL-DOMINANT, AND AUTOSOMAL RECESSIVE FORMS AND PRESENT STATE OF DNA STUDIES [J].

WALLGRENPETTERSSON, C ;

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