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Title
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De novo SCN1A mutations ara a major cause of severe myoclonic epilepsy of infancy
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Author
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Language
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English
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Source (journal)
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Human mutation. - New York, N.Y.
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Publication
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New York, N.Y.
:
2003
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ISSN
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1059-7794
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DOI
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10.1002/HUMU.10217
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Volume/pages
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21
(2003)
, p. 615-621
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ISI
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000183395500009
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Full text (Publisher's DOI)
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