Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients.
Hong Kong Med J
; 17(6): 500-2, 2011 Dec.
Article
in En
| MEDLINE
| ID: mdl-22147323
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Sodium Channels
/
Epilepsies, Myoclonic
/
Nerve Tissue Proteins
Type of study:
Diagnostic_studies
Limits:
Adolescent
/
Child
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Hong Kong Med J
Journal subject:
MEDICINA
Year:
2011
Document type:
Article
Affiliation country:
Country of publication: