Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B

Dominantly inherited GAA repeat expansions in FGF14 are a common cause of spinocerebellar ataxia (GAA-FGF14 ataxia; spinocerebellar ataxia 27B). Molecular confirmation of FGF14 GAA repeat expansions has thus far mostly relied on long-read sequencing, a technology that is not yet widely available in...

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Detalles Bibliográficos
Autores principales: Bonnet, Céline, Pellerin, David, Roth, Virginie, Clément, Guillemette, Wandzel, Marion, Lambert, Laëtitia, Frismand, Solène, Douarinou, Marian, Grosset, Anais, Bekkour, Ines, Weber, Frédéric, Girardier, Florent, Robin, Clément, Cacciatore, Stéphanie, Bronner, Myriam, Pourié, Carine, Dreumont, Natacha, Puisieux, Salomé, Iruzubieta, Pablo, Dicaire, Marie-Josée, Evoy, François, Rioux, Marie-France, Hocquel, Armand, La Piana, Roberta, Synofzik, Matthis, Houlden, Henry, Danzi, Matt C., Zuchner, Stephan, Brais, Bernard, Renaud, Mathilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272173/
https://www.ncbi.nlm.nih.gov/pubmed/37322040
http://dx.doi.org/10.1038/s41598-023-36654-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272173/
https://www.ncbi.nlm.nih.gov/pubmed/37322040
http://dx.doi.org/10.1038/s41598-023-36654-8

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