Divergent sodium channel defects in familial hemiplegic migraine

Familial hemiplegic migraine type 3 (FHM3) is a severe autosomal dominant migraine disorder caused by mutations in the voltage-gated sodium channel Na(V)1.1 encoded by SCN1A. We determined the functional consequences of three mutations linked to FHM3 (L263V, Q1489K, and L1649Q) in an effort to ident...

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Detalhes bibliográficos
Main Authors: Kahlig, Kristopher M., Rhodes, Thomas H., Pusch, Michael, Freilinger, Tobias, Pereira-Monteiro, José M., Ferrari, Michel D., van den Maagdenberg, Arn M. J. M., Dichgans, Martin, George, Alfred L.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2008
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2474506/
https://ncbi.nlm.nih.gov/pubmed/18621678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0711717105
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