Lack of SCN1A Mutations in Familial Febrile Seizures

スポンサーリンク

概要

論文の詳細を見る
2002-05-01

著者

関連論文

Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12
Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey : Identification of a Putative Locus on Chromosome 9q32-33
Lack of SCN1A Mutations in Familial Febrile Seizures
No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
Generalized Epilepsy with Febrile Seizures Plus (GEFS^+) : Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations
Dravet syndrome : Early clinical manifestations and cognitive outcome in 37 Italian patients
Electroclinical and Genetic Findings in a Family with Cortical Tremor, Myoclonus, and Epilepsy
Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms
Ictal EEG patterns in epilepsy with centro-temporal spikes

スポンサーリンク