A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility

While the role of common genetic variants in multiple sclerosis (MS) has been elucidated in large genome-wide association studies, the contribution of rare variants to the disease remains unclear. Herein, a whole-genome sequencing study in four affected and four healthy relatives of a consanguineous...

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Detalles Bibliográficos
Autores principales: Esposito, Federica, Osiceanu, Ana Maria, Sorosina, Melissa, Ottoboni, Linda, Bollman, Bryan, Santoro, Silvia, Bettegazzi, Barbara, Zauli, Andrea, Clarelli, Ferdinando, Mascia, Elisabetta, Calabria, Andrea, Zacchetti, Daniele, Capra, Ruggero, Ferrari, Maurizio, Provero, Paolo, Lazarevic, Dejan, Cittaro, Davide, Carrera, Paola, Patsopoulos, Nikolaos, Toniolo, Daniela, Sadovnick, A Dessa, Martino, Gianvito, De Jager, Philip L., Comi, Giancarlo, Stupka, Elia, Vilariño-Güell, Carles, Piccio, Laura, Martinelli Boneschi, Filippo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777893/
https://www.ncbi.nlm.nih.gov/pubmed/36553660
http://dx.doi.org/10.3390/genes13122392

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777893/
https://www.ncbi.nlm.nih.gov/pubmed/36553660
http://dx.doi.org/10.3390/genes13122392

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