De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy (Q40558873)
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scientific article published on June 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy |
scientific article published on June 2003 |
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De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy (English)
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Lieve Claes
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Berten Ceulemans
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Dominique Audenaert
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Katrien Smets
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Ann Löfgren
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Jurgen Del-Favero
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Sirpa Ala-Mello
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Barbara Plecko
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Salmo Raskin
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Paul Thiry
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Peter De Jonghe
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1 June 2003
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