A mutation in GABRB3 associated with Dravet syndrome.
Am J Med Genet A
; 173(8): 2126-2131, 2017 Aug.
Article
in En
| MEDLINE
| ID: mdl-28544625
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Base Sequence
/
Epilepsies, Myoclonic
/
Receptors, GABA-A
/
NAV1.1 Voltage-Gated Sodium Channel
Type of study:
Risk_factors_studies
Limits:
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2017
Document type:
Article
Affiliation country:
Vietnam
Country of publication:
United States