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

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

doi:10.1111/1346-8138.15513

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

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

Research output: Contribution to journal › Letter › peer-review

2 Citations (Scopus)

Original language	English
Pages (from-to)	e352-e354
Journal	Journal of Dermatology
Volume	47
Issue number	10
DOIs	https://doi.org/10.1111/1346-8138.15513
Publication status	Published - Oct 1 2020

ASJC Scopus subject areas

Dermatology

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10.1111/1346-8138.15513

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@article{d7305559e8fd478b8ebaea5b48ac61a3,

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

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

note = "Funding Information: We thank Dr Michihiro Kono (Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Japan) and Dr Akemi Ishida-Yamamoto (Department of Dermatology, Asahikawa Medical University, Japan) for their diagnostic advice.",

year = "2020",

month = oct,

day = "1",

doi = "10.1111/1346-8138.15513",

language = "English",

volume = "47",

pages = "e352--e354",

journal = "Journal of Dermatology",

issn = "0385-2407",

publisher = "Wiley-Blackwell",

number = "10",

}

TY - JOUR

T1 - Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene

T2 - Second Asian case

AU - Ikeda, Kenta

AU - Takeichi, Takuya

AU - Ito, Yasutoshi

AU - Kawakami, Yoshio

AU - Nakagawa, Yuki

AU - Naito, Seiko

AU - Yamasaki, Osamu

AU - Akiyama, Masashi

AU - Morizane, Shin

N1 - Funding Information: We thank Dr Michihiro Kono (Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Japan) and Dr Akemi Ishida-Yamamoto (Department of Dermatology, Asahikawa Medical University, Japan) for their diagnostic advice.

PY - 2020/10/1

Y1 - 2020/10/1

UR - http://www.scopus.com/inward/record.url?scp=85088556964&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85088556964&partnerID=8YFLogxK

U2 - 10.1111/1346-8138.15513

DO - 10.1111/1346-8138.15513

M3 - Letter

C2 - 32705719

AN - SCOPUS:85088556964

SN - 0385-2407

VL - 47

SP - e352-e354

JO - Journal of Dermatology

JF - Journal of Dermatology

IS - 10

ER -

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

ASJC Scopus subject areas

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