Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene: Second Asian case.

J Dermatol

Department of Dermatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Published: October 2020

Download full-text PDF	Source
http://dx.doi.org/10.1111/1346-8138.15513	DOI Listing

Publication Analysis

classical vohwinkel

vohwinkel syndrome

syndrome heterozygous

heterozygous pasp66his

pasp66his mutation

mutation gjb2

gjb2 gene

gene second

second asian

asian case

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