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

Esposito, F., Osiceanu, A. M., Sorosina, M., Ottoboni, L., Bollman, B., Santoro, S., Bettegazzi, B., Zauli, A., Clarelli, F., Mascia, E., Calabria, A., Zacchetti, D., Capra, R., Ferrari, M., Provero, P., Lazarevic, D., Cittaro, D., Carrera, P., Patsopoulos, N., … Martinelli Boneschi, F. (2022). A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility. Genes, 13(12), 2392. https://doi.org/10.3390/genes13122392
Authors:
Federica Esposito
Ana Maria Osiceanu
Melissa Sorosina
Linda Ottoboni
Bryan Bollman
Silvia Santoro
Barbara Bettegazzi
Andrea Zauli
Ferdinando Clarelli
Elisabetta Mascia
Andrea Calabria
Daniele Zacchetti
Ruggero Capra
Maurizio Ferrari
Paolo Provero
Dejan Lazarevic
Davide Cittaro
Paola Carrera
Nikolaos Patsopoulos
Daniela Toniolo
A Dessa Sadovnick
Gianvito Martino
Philip L De Jager
Giancarlo Comi
Elia Stupka
Carles Vilariño-Güell
Laura Piccio
Filippo Martinelli Boneschi
Affiliated Authors:
Philip L De Jager
Columbia Affiliation:
Subjects:
Genetic Predisposition to Disease (MeSH)
Multiple Sclerosis (MeSH)
Author Keywords:
multiple sclerosis
neurology
sequencing
rare variants
elink
Publication Type:
Article
Unique ID:
10.3390/genes13122392
PMID:
36553660
DOI:
10.3390/genes13122392
Journal:
Genes
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
View Web of Science Record

Record Created: