Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
スポンサーリンク
概要
著者
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Yang Zhixian
Department Of Pediatrics Peking University First Hospital
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Sun Huihui
Department Of Pediatrics Peking University First Hospital
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Liu Xiaoyan
Department Of Pediatrics Peking University First Hospital
関連論文
- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Clinical and biochemical studies on Chinese patients with methylmalonic acidumia
- Genetic studies on SURF1 mutations in Chinese patients with mitochondrial encephalopathy
- A Clinical Survey of 65 Patients with Leigh Syndrome
- Modulating effect of hydrogen sulfide on gamma-aminobutyric acid B receptor in recurrent febrile seizures in rats
- Phenylketonuria in China : From Neonatal Screening to Laboratory Study
- A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood
- SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus
- Alpers syndrome with prominent white matter changes
- Childhood absence epilepsy : Elctroclinical features and diagnostic criteria
- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Epilepsy in children with methylmalonic acidemia : Electroclinical features and prognosis