Identification of Copy Number Variations in Familial Hemiplegic Migraine Genes in Suspected Hemiplegic Migraine Patients

<b>Background</b>: Familial hemiplegic migraine (FHM) is a rare and severe form of migraine disorder featuring aura symptoms that include hemiplegia during attacks. While pathogenic missense variants in <i>CACNA1A</i>, <i>ATP1A2</i>, and <i>SCN1A</i> can cause FHM or its sporadic form, they explain...

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Detalhes bibliográficos

Principais autores:	Thais Zielke, Heidi G. Sutherland, Neven Maksemous, Robert A. Smith, Lyn R. Griffiths
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2026-04-01
Colecção:	Biomedicines
Assuntos:	familial hemiplegic migraine hemiplegic migraine copy number variations (CNVs) <i>CACNA1A</i> <i>ATP1A2</i> <i>SCN1A</i>
Acesso em linha:	https://www.mdpi.com/2227-9059/14/5/954
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