Erythrokeratodermia variabilis et progressiva with a rare GJB3 mutation
Author:
Affiliation:
1. Department of DermatologyHamamatsu University School of Medicine HamamatsuJapan
2. Department of Pediatrics Hamamatsu University School of Medicine Hamamatsu Japan
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15206
Reference5 articles.
1. Connexin disorders of the skin
2. Two de novo GJA1 mutation in two sporadic patients with erythrokeratodermia variabilis et progressiva
3. Erythrokeratodermia variabilis: First Japanese case documentingGJB3mutation
4. Erythrokeratoderma variabilis without GJB3 or GJB4 mutation: a review of Japanese patients
5. An Unusual Missense Mutation in the GJB3 Gene Resulting in Severe Erythrokeratodermia Variabilis
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Connexin Gene (GJB3) Mutation in a Chinese Family With Erythrokeratodermia Variabilis, Ichthyosis and Nonsyndromic Hearing Loss: Case Report and Mutations Update;Frontiers in Genetics;2022-05-23
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