Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: identification of a recurrent p.P25L mutation in KRT5 in four affected family members.
Br J Dermatol
; 174(3): 633-5, 2016 Mar.
Article
in En
| MEDLINE
| ID: mdl-26286811
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Epidermolysis Bullosa Simplex
/
Mutation, Missense
/
Alopecia
/
Keratin-5
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
Language:
En
Journal:
Br J Dermatol
Year:
2016
Document type:
Article
Affiliation country:
Japón
Country of publication:
Reino Unido