Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

被引：244

作者：

Liu, XZ

Walsh, J

Tamagawa, Y

Kitamura, K

Nishizawa, M

Steel, KP

Brown, SDM

机构：

[1] MRC, MOUSE GENOME CTR, HARWELL OX11 0RD, BERKS, ENGLAND

[2] MRC, MAMMALIAN GENET UNIT, HARWELL OX11 0RD, BERKS, ENGLAND

[3] JICHI MED SCH, DEPT OTOLARYNGOL, MINAMI KAWACHI, TOCHIGI 32904, JAPAN

[4] JICHI MED SCH, DEPT NEUROL, MINAMI KAWACHI, TOCHIGI 32904, JAPAN

[5] MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND

来源：

NATURE GENETICS | 1997年 / 17卷 / 03期

关键词：

D O I：

10.1038/ng1197-268

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：268 / 269

页数：2

共 11 条

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