Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference37 articles.
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4. Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions;Biervert;Hum. Genet.,1999
5. A potassium channel mutation in neonatal human epilepsy;Biervert;Science,1998
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