Publication | Closed Access
Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations
45
Citations
28
References
2013
Year
Scn1a MutationsDravet SyndromeAllelic VariantGenetic DisorderGeneticsInherited Metabolic DiseasePathologyDisease Gene IdentificationMedicineClinical GeneticsChinese Patients
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