Japanese sporadic case of erythrokeratodermia variabilis caused by the connexin-30.3 ( GJB4 ) mutation: Is Glycine 12 a mutational hotspot in the connexin family?
Yoshikata-Isokawa, Yumie, Itoh, Munenari, Nakagawa, HidemiVolume:
43
Language:
english
Journal:
The Journal of Dermatology
DOI:
10.1111/1346-8138.13277
Date:
July, 2016
File:
PDF, 270 KB
english, 2016