Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes

Hemiplegic migraine (HM) is a rare subtype of migraine with aura. Given that causal missense mutations in the voltage-gated calcium channel α1A subunit gene CACNA1A have been identified in a subset of HM patients, we investigated whether HM patients without a mutation have an increased burden of suc...

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Detalles Bibliográficos
Autores principales: Maksemous, Neven, Harder, Aster V. E., Ibrahim, Omar, Vijfhuizen, Lisanne S., Sutherland, Heidi, Pelzer, Nadine, de Boer, Irene, Terwindt, Gisela M., Lea, Rodney A., van den Maagdenberg, Arn M. J. M., Griffiths, Lyn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122627/
https://www.ncbi.nlm.nih.gov/pubmed/36786913
http://dx.doi.org/10.1007/s12035-023-03255-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122627/
https://www.ncbi.nlm.nih.gov/pubmed/36786913
http://dx.doi.org/10.1007/s12035-023-03255-5

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