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Article

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

The Journal of dermatology - 1 Oct 2020

Ikeda Kenta, Takeichi Takuya, Ito Yasutoshi, Kawakami Yoshio, Nakagawa Yuki, Naito Seiko, Yamasaki Osamu, Akiyama Masashi, Morizane Shin

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Share to Abnormalities, Multiple
Share to Connexin 26
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Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hand Deformities, Congenital

Share to Hearing Loss, Sensorineural

Share to Keratoderma, Palmoplantar

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Identifiers

PMID: 32705719
DOI: 10.1111/1346-8138.15513

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene: Second Asian case.PMID 32705719Read ↗

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Palmoplantar keratoderma with deafness due to GJB2 mutation can develop ichthyosiform symptoms: a case report.Semantic proximity Read ↗

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