Digenic mutations in severe myoclonic epilepsy of infancy-Reference-Cited by-同舟云学术

Digenic mutations in severe myoclonic epilepsy of infancy

Published:2009-08 Issue:2-3 Volume:85 Page:300-304
ISSN:0920-1211
Container-title:Epilepsy Research
language:en
Short-container-title:Epilepsy Research

Author:

Bolszak Maija,Anttonen Anna-Kaisa,Komulainen Tuomas,Hinttala Reetta,Pakanen Salla,Sormunen Raija,Herva Riitta,Lehesjoki Anna-Elina,Majamaa Kari,Rantala Heikki,Uusimaa Johanna

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference17 articles.

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2. Severe myoclonic epilepsy and mitochondrial cytopathy;Castro-Gago;Childs Nerv. Syst.,1997

3. Les épilepsies graves de l’enfant;Dravet;La Vie Médicale,1978

4. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2;Escayg;Nat. Genet.,2000

5. Diagnosis in severe myoclonic epilepsy in childhood: study of 13 cases;Fernández-Jaén;Rev. Neurol.,1998

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