SCN2A mutation associated with neonatal epilepsy,...

Neurology 2010 / 10 Vol. 75; Iss. 16

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

Liao, Y., Anttonen, A.- K., Liukkonen, E., Gaily, E., Maljevic, S., Schubert, S., Bellan-Koch, A., Petrou, S., Ahonen, V. E., Lerche, H., Lehesjoki, A.- E.
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Volume:
75
Language:
english
Journal:
Neurology
DOI:
10.1212/wnl.0b013e3181f8812e
Date:
October, 2010
File:
PDF, 1.55 MB
english, 2010
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