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Rare mutations and common polymorphisms of the epilepsies : Ion channels disease mechanisms and response to treatment| old_uid | 1297 |
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| title | Rare mutations and common polymorphisms of the epilepsies : Ion channels disease mechanisms and response to treatment |
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| start_date | 2006/05/22 |
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| schedule | 12h |
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| online | no |
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| location_info | salle 505 |
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| details | Séminaire organisé par l’U739 de l’Hôpital Pitié - Salpêtrière |
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| summary | Most Mendelian epilepsy genes code for ion channels, but the contribution of common single nucleotide polymorphisms is unknown. Dimitri Kullmann will present work on calcium and potassium channel mutations associated with ataxia and epilepsy, and a sodium channel polymorphism associated with differences in antiepileptic drug dosage. |
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| responsibles | <not specified> |
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