A case of PAPASH syndrome in a young man carrying a novel heterozygote missense variant in PSTPIP1.
J Eur Acad Dermatol Venereol
; 35(7): e439-e440, 2021 Jul.
Article
in En
| MEDLINE
| ID: mdl-33587775
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pyoderma Gangrenosum
/
Mutation, Missense
Limits:
Humans
/
Male
Language:
En
Journal:
J Eur Acad Dermatol Venereol
Journal subject:
DERMATOLOGIA
/
DOENCAS SEXUALMENTE TRANSMISSIVEIS
Year:
2021
Document type:
Article
Affiliation country:
Germany