Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan

Tomoko Miyake; Ken Natsuga; Takatsune Umayahara; Seiko Naito; Junko Yoshimoto; Akemi Senoo; Han Tang Wang; Chao Kai Hsu; Osamu Yamasaki; Shin Morizane

doi:10.1111/1346-8138.16195

Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan

Tomoko Miyake, Ken Natsuga, Takatsune Umayahara, Seiko Naito, Junko Yoshimoto, Akemi Senoo, Han Tang Wang, Chao Kai Hsu, Osamu Yamasaki, Shin Morizane

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

1 Citation (Scopus)

Original language	English
Journal	Journal of Dermatology
DOIs	https://doi.org/10.1111/1346-8138.16195
Publication status	Accepted/In press - 2021

ASJC Scopus subject areas

Dermatology

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10.1111/1346-8138.16195

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@article{a14a1c2910274fd09157ee03f9d4862f,

title = "Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan",

author = "Tomoko Miyake and Ken Natsuga and Takatsune Umayahara and Seiko Naito and Junko Yoshimoto and Akemi Senoo and Wang, {Han Tang} and Hsu, {Chao Kai} and Osamu Yamasaki and Shin Morizane",

year = "2021",

doi = "10.1111/1346-8138.16195",

language = "English",

journal = "Journal of Dermatology",

issn = "0385-2407",

publisher = "Wiley-Blackwell",

}

TY - JOUR

T1 - Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan

AU - Miyake, Tomoko

AU - Natsuga, Ken

AU - Umayahara, Takatsune

AU - Naito, Seiko

AU - Yoshimoto, Junko

AU - Senoo, Akemi

AU - Wang, Han Tang

AU - Hsu, Chao Kai

AU - Yamasaki, Osamu

AU - Morizane, Shin

PY - 2021

Y1 - 2021

UR - http://www.scopus.com/inward/record.url?scp=85117103781&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85117103781&partnerID=8YFLogxK

U2 - 10.1111/1346-8138.16195

DO - 10.1111/1346-8138.16195

M3 - Letter

C2 - 34658058

AN - SCOPUS:85117103781

SN - 0385-2407

JO - Journal of Dermatology

JF - Journal of Dermatology

ER -

Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan

ASJC Scopus subject areas

Access to Document

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