Open AccessSingle nucleotide variants in the SCN1A gene and their relation to the development of type 3 familial hemiplegic migraine
Author(s) -
Bárbara Prevital dos Santos,
Bruna Maschi,
Gabriela Rosa Campos,
Giovanna Correa Rossi,
Giulia Eloah de Pádua Ribeiro,
Glória Maria Doroso Volpato,
Júlia Vitturi,
Lara Schiavão de Carvalho,
Larissa Carolina Rosin,
Letícia Amelotti Coelho,
Rubem Soter Neto,
Valéria Aparecida Bello,
Aline Vitali da Silva,
Regina Célia Poli Frederico
Publication year - 2022
Language(s) - English
Resource type - Journals
ISSN - 2763-6178
DOI - 10.48208/headachemed.2022.supplement.17
Subject(s) - familial hemiplegic migraine , neuroscience , ion channel , biology , missense mutation , migraine , genetics , gene , mutation , medicine , migraine with aura , receptor , aura