スポンサーリンク
Department of Pediatrics, Peking University First Hospital | 論文
- Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bε (eIF2Bε) identified in Chinese patients with vanishing white matter disease
- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Meta-Analysis of Randomized Controlled Trials on Treatment of Pulmonary Arterial Hypertension
- Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)
- Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease
- Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay
- Epilepsy in children with methylmalonic acidemia : Electroclinical features and prognosis
- Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutations