The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics

被引：42

作者：

Chomyn, A ^{[1
]}

机构：

[1] CALTECH, Div Biol, Pasadena, CA 91125 USA

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 62卷 / 04期

关键词：

D O I：

10.1086/301813

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：745 / 751

页数：7

共 28 条

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