Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)

被引：92

作者：

Mohiddin, SA

Ahmed, ZM

Griffith, AJ

Tripodi, D

Friedman, TB

Fananapazir, L

Morell, RJ

机构：

[1] NIDCD, Sect Human Genet, Mol Genet Lab, NIH, Rockville, MD 20850 USA

[2] NIDCD, Sect Gene Struct & Funct, Genet Mol Lab, NIH, Rockville, MD 20850 USA

[3] NHLBI, Cardiovasc Branch, NIH, Bethesda, MD 20892 USA

[4] NIDCD, Hearing Sect, Neurootol Branch, NIH, Rockville, MD 20850 USA

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 04期

关键词：

D O I：

10.1136/jmg.2003.011973

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：309 / 314

页数：6

共 39 条

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