De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy (Q40558873)
scientific article published on June 2003
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Current Data About De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy
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other details
description scientific article published on June 2003

External Links
(P356) 10.1002/HUMU.10217
(P698) 12754708