Coexistence of KRT14 and KRT5 mutations in a Polish patient with epidermolysis bullosa simplex
Br J Dermatol
.
2014 Feb;170(2):468-9.
doi: 10.1111/bjd.12624.
Authors
K Wertheim-Tysarowska
1
,
J Sota
,
A Kutkowska-Kaźmierczak
,
K Woźniak
,
J Bal
,
C Kowalewski
Affiliation
1
Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, Warsaw, 01-211, Poland. katarzyna.wertheim@imid.med.pl.
PMID:
24024749
DOI:
10.1111/bjd.12624
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child, Preschool
Epidermolysis Bullosa Simplex / genetics*
Humans
Keratin-14 / genetics*
Keratin-5 / genetics*
Male
Mutation / genetics*
Pedigree
Substances
Keratin-14
Keratin-5