TY  - JOUR
AU  - Gomez Pinedo, Ulises
AU  - Matías-Guiu Guía, Jorge
AU  - Torre Fuentes, Laura
AU  - Montero Escribano, Paloma
AU  - Hernández Lorenzo, Laura
AU  - Pytel, Vanessa
AU  - Maietta, Paolo
AU  - Álvarez de Andrés, Sara
AU  - Sanclemente Alamán, Inmaculada
AU  - Moreno Jimenez, Lidia
AU  - Ojeda Hernández, Doddy Denise
AU  - Villar-Gómez, Natalia
AU  - Benito-Martin, María Soledad
AU  - Selma-Calvo, Belén 
AU  - Matías Guiu, Jordi
AU  - Vidorreta-Ballesteros, Lucía
AU  - Madrid González, Ricardo
PY  - 2022
DO  - 10.1016/j.nrleng.2022.07.002
SN  - 2173-5808
UR  - https://hdl.handle.net/20.500.14352/97475
T2  - Neurología
AB  - Genomic studies have identified numerous genetic variants associated with sus-ceptibility to multiple sclerosis (MS); however, each one explains only a small percentage of therisk of developing the disease. These variants are located in genes involved...
LA  - eng
M2  - 1
KW  - Familial multiple sclerosis
KW  - Genetics
KW  - HOG cells
KW  - Myelination
KW  - TNFRSF1A
KW  - Whole-exome sequencing
TI  - Variant rs4149584 (R92Q) of the TNFRSF1A gene in patients with familial multiple sclerosis
TY  - journal article
ER  -