Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

VERHOEVEN K; KIRSCHHOFER K; LEGAN P K; HUGHES D C; CHEN A; SOMERS T; WACHTLER F; KIMBERLING W J; VAN CAMP G

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J-GLOBAL ID：200902182713673636 Reference number：98A0567152

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

ヒトα-テクトリン突然変異は常染色体優性非症候群的聴覚障害を起こす

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Material：
Volume： 19 Issue： 1 Page： 60-62 Publication year： May. 1998
JST Material Number： W0430A ISSN： 1061-4036 Document type： Article
Article type：短報 Country of issue： United States (USA) Language： ENGLISH (EN)

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Structure and chemistry of genes , Otorhinolaryngologic diagnosis

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