An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation

BACKGROUND: Mutations in the CACNA1A gene encoding the voltage-gated calcium channel α1A subunit have been identified in patients with autosomal dominantly inherited neurological disorders, including spinocerebellar ataxia type 6 (SCA6) and familial hemiplegic migraine type 1 (FHM1). In order to inv...

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Detalles Bibliográficos
Autores principales: Kono, Satoshi, Terada, Tatsuhiro, Ouchi, Yasuomi, Miyajima, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633947/
https://www.ncbi.nlm.nih.gov/pubmed/26675662
http://dx.doi.org/10.1016/j.bbacli.2014.09.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633947/
https://www.ncbi.nlm.nih.gov/pubmed/26675662
http://dx.doi.org/10.1016/j.bbacli.2014.09.005

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