De Novo SCN8A Mutation Identified by Whole-Exome Sequencing...

Journal of Child Neurology 2014 / 12 Vol. 29; Iss. 12

De Novo SCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders

Vaher, U., Noukas, M., Nikopensius, T., Kals, M., Annilo, T., Nelis, M., Ounap, K., Reimand, T., Talvik, I., Ilves, P., Piirsoo, A., Seppet, E., Metspalu, A., Talvik, T.
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Volume:
29
Language:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073813511300
Date:
December, 2014
File:
PDF, 551 KB
english, 2014
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