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Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients.
Mak, Chloe M; Chan, K Y; Yau, Eric K C; Chen, Sammy P L; Siu, W K; Law, C Y; Lam, C W; Chan, Albert Y W.
Affiliation
  • Mak CM; Kowloon West Cluster Laboratory Genetic Service, Chemical Pathology Laboratory, Department of Pathology, Princess Margaret Hospital, Laichikok, Hong Kong. makm@ha.org.hk
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: Hong Kong Country of publication: China
Search on Google
Add to My VHL
Print
XML
PubMed Links

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: Hong Kong Country of publication: China