A new SPINK5 mutation in a patient with Netherton syndrome: a case report.
Pediatr Dermatol
; 29(4): 521-2, 2012.
Article
in En
| MEDLINE
| ID: mdl-21692842
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ichthyosiform Erythroderma, Congenital
/
Point Mutation
/
Proteinase Inhibitory Proteins, Secretory
/
Netherton Syndrome
Limits:
Adult
/
Humans
/
Male
Language:
En
Journal:
Pediatr Dermatol
Year:
2012
Document type:
Article
Affiliation country:
Italy
Country of publication:
United States