Literature DB >> 18554359

Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy.

Huihui Sun, Yuehua Zhang, Jianmin Liang, Xiaoyan Liu, Xiuwei Ma, Jiong Qin, Yu Qi, Xiru Wu.   

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Year:  2008        PMID： 18554359     DOI： 10.1111/j.1528-1167.2008.01549_2.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN： 0013-9580            Impact factor:   5.864


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  3 in total

1.  Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases.

Authors:  Chunhong Chen; Fang Fang; Xu Wang; Junlan Lv; Xiaohui Wang; Hong Jin
Journal:  Front Mol Neurosci       Date:  2022-04-28       Impact factor: 5.639

2.  Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients.

Authors:  Meral Ozmen; Cengiz Dilber; Burak Tatlı; Nur Aydınlı; Mine Calışkan; Barış Ekici
Journal:  Ann Indian Acad Neurol       Date:  2011-07       Impact factor: 1.383

3.  Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study.

Authors: 
Journal:  Iran J Child Neurol       Date:  2013
  3 in total

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