Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.
Genet Couns
; 24(3): 273-7, 2013.
Article
in En
| MEDLINE
| ID: mdl-24341141
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Glucuronosyltransferase
/
Crigler-Najjar Syndrome
/
Gilbert Disease
Limits:
Female
/
Humans
/
Newborn
Country/Region as subject:
Asia
Language:
En
Journal:
Genet Couns
Journal subject:
ETICA
/
GENETICA MEDICA
Year:
2013
Document type:
Article
Affiliation country:
Turquía
Country of publication:
Suiza