Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A

Molecular syndromology

Steffen Syrbe¹ 

关键词: Brain atrophy;    Channelopathy;    Early-onset epileptic encephalopathy;    Epilepsy;   

DOI  :  10.1159/000447526

学科分类：基础医学

来源: S Karger AG

【 授权许可】

CC BY