Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine

Familial hemiplegic migraine (FHM) is a severe neurogenetic disorder for which three causal genes, CACNA1A, SCN1A, and ATP1A2, have been implicated. However, more than 80% of referred diagnostic cases of hemiplegic migraine (HM) are negative for exonic mutations in these known FHM genes, suggesting...

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Detalles Bibliográficos
Autores principales: Maksemous, Neven, Blayney, Claire D., Sutherland, Heidi G., Smith, Robert A., Lea, Rod A., Tran, Kim Ngan, Ibrahim, Omar, McArthur, Jeffrey R., Haupt, Larisa M., Cader, M. Zameel, Finol-Urdaneta, Rocio K., Adams, David J., Griffiths, Lyn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345121/
https://www.ncbi.nlm.nih.gov/pubmed/35928792
http://dx.doi.org/10.3389/fnmol.2022.892820

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345121/
https://www.ncbi.nlm.nih.gov/pubmed/35928792
http://dx.doi.org/10.3389/fnmol.2022.892820

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