Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1.
BMC Med Genet
; 18(1): 20, 2017 Feb 23.
Article
in En
| MEDLINE
| ID: mdl-28231770
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Telangiectasia, Hereditary Hemorrhagic
/
Promoter Regions, Genetic
/
Endoglin
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
BMC Med Genet
Journal subject:
GENETICA MEDICA
Year:
2017
Document type:
Article
Affiliation country:
España
Country of publication:
Reino Unido