A mutation (2314delG) in the usher syndrome type IIA gene: High prevalence and phenotypic variation

被引：65

作者：

Liu, XZ

Hope, C

Liang, CY

Zou, JM

Xu, LR

Cole, T

Mueller, RF

Bundey, S

Nance, W

Steel, KP

Brown, SDM

机构：

[1] Virginia Commonwealth Univ, Med Coll Virginia, Dept Human Genet, Richmond, VA 23298 USA

[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Otolaryngol, Richmond, VA 23298 USA

[3] W China Univ Med Sci, Dept Otolaryngol, Chengdu 610041, Peoples R China

[4] W China Univ Med Sci, Dept Ophthalmol, Chengdu 610041, Peoples R China

[5] MRC, Inst Hearing Res, Nottingham, England

[6] St James Univ Hosp, Dept Clin Genet, Leeds, W Yorkshire, England

[7] Univ Birmingham, Clin Genet Unit, Birmingham, W Midlands, England

[8] United Kingdom Mouse Genome Ctr, Harwell, Oxon, England

[9] MRC, Mammalian Genet Unit, Harwell, Oxon, England

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 64卷 / 04期

关键词：

D O I：

10.1086/302332

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1221 / 1225

页数：5

共 12 条

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