A novel nemaline myopathy in the Amish caused by a mutation in troponin T1.

被引：253

作者：

Johnston, JJ

Kelley, RI

Crawford, TO

Morton, DH

Agarwala, R

Koch, T

Schäffer, AA

Francomano, CA

Biesecker, LG

机构：

[1] NHGRI, NIH, Bethesda, MD 20892 USA

[2] Johns Hopkins Univ, Baltimore, MD 21218 USA

[3] Clin Special Children, Strasburg, PA 17579 USA

[4] Natl Lib Med, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA

[5] Konrad Zuse Zentrum Informationstech, Berlin, Germany

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04期

关键词：

D O I：

10.1086/303089

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

229

引用

页码：54 / 54

页数：1

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