Novel KCNQ2 and...

Human Mutation 2014 / 03 Vol. 35; Iss. 3

Novel KCNQ2 and KCNQ3 Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin-1A

Soldovieri, Maria Virginia, Boutry-Kryza, Nadia, Milh, Mathieu, Doummar, Diane, Heron, Benedicte, Bourel, Emilie, Ambrosino, Paolo, Miceli, Francesco, De Maria, Michela, Dorison, Nathalie, Auvin, Step
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Volume:
35
Language:
english
Journal:
Human Mutation
DOI:
10.1002/humu.22500
Date:
March, 2014
File:
PDF, 961 KB
english, 2014
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