Novel and recurrent C1 inhibitor gene mutations in nine Japanese patients with hereditary angioedema.
J Dermatol Sci
; 68(1): 68-70, 2012 Oct.
Article
in En
| MEDLINE
| ID: mdl-22831796
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Complement C1 Inactivator Proteins
/
Angioedemas, Hereditary
/
Mutation
Limits:
Adult
/
Aged
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Journal:
J Dermatol Sci
Journal subject:
DERMATOLOGIA
Year:
2012
Document type:
Article
Country of publication:
Netherlands