| 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. | |
| 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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| 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 (Publishers DOI) |
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