S159P mutation of keratin 10 gene causes severe form of epidermolytic hyperkeratosis
J Eur Acad Dermatol Venereol
.
2016 Oct;30(10):e102-e104.
doi: 10.1111/jdv.13345.
Epub 2015 Sep 15.
Authors
P-J Chen
1
,
C-X Li
1
2
,
J Wen
3
,
Y-S Peng
1
,
K Zeng
4
,
S-Q Zhang
5
6
,
X Tian
5
6
,
X-B Zhang
7
8
Affiliations
1
Department of Dermatology, Nanfang Hospital, South Medical University, Guangzhou, Guangdong Provice, China.
2
Department of Dermatology, Dongguan No.6 People's Hospital, Dongguan, Guangdong Provice, China.
3
Department of Dermatology, Guangdong No.2 Provincial People's Hospital, Guangzhou, Guangdong Provice, China.
4
Department of Dermatology, Nanfang Hospital, South Medical University, Guangzhou, Guangdong Provice, China. npfkzk@163.com.
5
Department of Dermatology, Guangzhou Institute of Dermatology, Guangzhou, Guangdong Provice, China.
6
Institute of Dermatology, Guangzhou Medical University, Guangzhou, Guangdong Provice, China.
7
Department of Dermatology, Guangzhou Institute of Dermatology, Guangzhou, Guangdong Provice, China. zxibao@126.com.
8
Institute of Dermatology, Guangzhou Medical University, Guangzhou, Guangdong Provice, China. zxibao@126.com.
PMID:
26373619
DOI:
10.1111/jdv.13345
No abstract available
Publication types
Letter
MeSH terms
Female
Humans
Hyperkeratosis, Epidermolytic / genetics*
Keratin-10 / genetics*
Male
Mutation*
Substances
KRT10 protein, human
Keratin-10