The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. (Q48223071)
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scientific article published in May 2007
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. |
scientific article published in May 2007 |
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The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. (English)
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Martin Dichgans
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Gisela M Terwindt
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Michel D Ferrari
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Kaate R J Vanmolkot
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Elena Babini
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Boukje de Vries
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Anine H Stam
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Tobias Freilinger
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Lisa Norris
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Joost Haan
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Rune R Frants
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Nabih M Ramadan
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Arn M J M van den Maagdenberg
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1 May 2007
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