Case of inherited epidermolysis bullosa simplex with KLHL24 gene mutation in Japan
J Dermatol
.
2022 Jan;49(1):e24-e25.
doi: 10.1111/1346-8138.16195.
Epub 2021 Oct 18.
Authors
Tomoko Miyake
1
,
Ken Natsuga
2
,
Takatsune Umayahara
3
,
Seiko Naito
3
,
Junko Yoshimoto
4
,
Akemi Senoo
3
,
Han-Tang Wang
5
6
,
Chao-Kai Hsu
5
6
,
Osamu Yamasaki
1
,
Shin Morizane
1
Affiliations
1
Department of Dermatology, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama, Japan.
2
Department of Dermatology, Hokkaido University, Sapporo, Japan.
3
Division of Dermatology, Okayama Red Cross Hospital, Okayama, Japan.
4
Department of Pediatrics, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama, Japan.
5
Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
6
International Center for Wound Repair and Regeneration (iWRR), National Cheng Kung University, Tainan, Taiwan.
PMID:
34658058
DOI:
10.1111/1346-8138.16195
No abstract available
Publication types
Letter
MeSH terms
Epidermolysis Bullosa Simplex* / genetics
Epidermolysis Bullosa*
Humans
Japan
Mutation
Pedigree