D66H mutation in GJB2 gene in a Chinese family with classical Vohwinkel syndrome.

Qiu, Ying; Wang, Zhanxiang; Chen, Nan; Song, Yali; Wang, Zhenying; Zhang, Li

Qiu, Ying; Wang, Zhanxiang; Chen, Nan; Song, Yali; Wang, Zhenying; Zhang, Li.

Indian J Dermatol Venereol Leprol ; 2012 Sept-Oct; 78(5): 640-642

Article in English | IMSEAR | ID: sea-141183

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Full text: Available Index: IMSEAR (South-East Asia) Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2012 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2012 Type: Article