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Mutations in GABA(A) receptor subunits associated with genetic epilepsies
Mutations in inhibitory GABA(A) receptor subunit genes (GABRA1, GABRB3, GABRG2 and GABRD) have been associated with genetic epilepsy syndromes including childhood absence epilepsy (CAE), juvenile myoclonic epilepsy (JME), pure febrile seizures (FS), generalized epilepsy with febrile seizures plus (G...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Blackwell Science Inc
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2901974/ https://ncbi.nlm.nih.gov/pubmed/20308251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2010.186999 |
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