P39 – 2771: Variable phenotype in epilepsy caused by KCNQ2...

P39 – 2771: Variable phenotype in epilepsy caused by KCNQ2 mutations

Jansen, K., Dereymaeker, A., De Waele, L., Lagae, L.
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Volume:
19
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/S1090-3798(15)30352-4
Date:
May, 2015
File:
PDF, 80 KB
english, 2015
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