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

作者

Qiu, Y;Wang, ZX;Chen, N;Song, YL;Wang, ZY;Zhang, L

作者单位

[Wang, Zhanxiang; Chen, Nan; Song, Yali; Wang, Zhenying; Zhang, Li] Shandong Univ, Dept Dermatol, Prov Hosp, Jinan, Shandong, Peoples R China.;-;[Qiu, Ying] Jining First Peoples Hosp, Dept Dermatol, Jining, Shandong, Peoples R China.

摘要

关键词

DOMINANT CONNEXIN DISORDERS; MISSENSE MUTATION; MUTILATING KERATODERMA; DEAFNESS

基本信息

所属机构:

归属医师: 宋亚丽王震英张莉陈楠

PMID：22960825

UT：000308857700019

刊名:INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY

年，卷(期):2012年78卷5期

页码：640-U193

DOI：10.4103/0378-6323.100595

附件：

收录: SCIE