Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report

RATIONALE: Familial hemiplegic migraine (FHM) is a rare, autosomal dominant migraine with aura. CACNA1A encodes the α1A subunit of P/Q-type voltage-gated calcium channels, and its mutations have been associated with a wide spectrum of episodic and chronic neurological disorders, including FHM type 1...

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Detalles Bibliográficos
Autores principales: Luan, Huiyan, Zhang, Lei, Zhang, Sijin, Zhang, Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702007/
https://www.ncbi.nlm.nih.gov/pubmed/34941060
http://dx.doi.org/10.1097/MD.0000000000028141

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702007/
https://www.ncbi.nlm.nih.gov/pubmed/34941060
http://dx.doi.org/10.1097/MD.0000000000028141

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