Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings

被引：9

作者：

Arellano, B ^{[1
]}

Pera, A ^{[1
]}

Ramírez-Camacho, R ^{[1
]}

Villamar, M ^{[1
]}

Trinidad, A ^{[1
]}

Garcia, JR ^{[1
]}

Moreno, F ^{[1
]}

Hernández-Chico, C ^{[1
]}

机构：

[1] Hosp Puerta Hierro, Serv Otorrinolaringol, Madrid 28035, Spain

来源：

CLINICAL GENETICS | 2005年 / 67卷 / 05期

关键词：

D O I：

10.1111/j.1399-0004.2005.00432.x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：438 / 440

页数：3

共 11 条

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