G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome
Xie, Ming-xing, Yang, Wei-ping, Luo, Hao-jie, Ismail, Ferina, Hao, Yang-yang, Yang, Jian-qiangLanguage:
english
Journal:
The Journal of Dermatology
DOI:
10.1111/1346-8138.14727
Date:
December, 2018
File:
PDF, 533 KB
english, 2018