Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding region.
Hum Hered
; 42(5): 298-301, 1992.
Article
in En
| MEDLINE
| ID: mdl-1459574
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Complement C1 Inactivator Proteins
/
Angioedema
/
Mutation
Type of study:
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Hum Hered
Year:
1992
Document type:
Article
Affiliation country:
Reino Unido
Country of publication:
Suiza