A novel insertion (c.1098dupT) in the albumin gene causes analbuminemia in a consanguineous family.
Eur J Med Genet
; 62(2): 144-148, 2019 Feb.
Article
in En
| MEDLINE
| ID: mdl-29981851
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hypoalbuminemia
/
Serum Albumin, Human
/
Mutation
Type of study:
Etiology_studies
/
Prognostic_studies
Limits:
Adult
/
Aged
/
Female
/
Humans
/
Male
Language:
En
Journal:
Eur J Med Genet
Journal subject:
GENETICA MEDICA
Year:
2019
Document type:
Article
Affiliation country:
Italy
Country of publication:
Netherlands