TY  - JOUR
AU  - Alcina, Antonio
AU  - Fedetz, Maria
AU  - Vidal-Cobo, Isabel
AU  - Andres-Leon, Eduardo
AU  - Garcia-Sanchez, Maria-Isabel
AU  - Barroso-Del-Jesus, Alicia
AU  - Eichau, Sara
AU  - Gil-Varea, Elia
AU  - Luisa-Maria Villar
AU  - Saiz, Albert
AU  - Leyva, Laura
AU  - Vandenbroeck, Koen
AU  - Otaegui, David
AU  - Izquierdo, Guillermo
AU  - Comabella, Manuel
AU  - Urcelay, Elena
AU  - Matesanz, Fuencisla
PY  - 2022
DO  - 10.1093/hmg/ddac009
UR  - http://hdl.handle.net/10668/19785
T2  - Human molecular genetics
AB  - Multiple sclerosis (MS) is a complex and demyelinating disease of the central nervous system. One of the challenges of the post-genome-wide association studies (GWAS) era is to understand the molecular basis of statistical associations to reveal gene...
LA  - en
PB  - Oxford University Press
KW  - DNA-binding proteins
KW  - Multiple sclerosis
KW  - Polymorphism, single nucleotide
KW  - DNA-binding proteins
KW  - Genetic predisposition to disease
KW  - Genome-wide association study
KW  - Humans
KW  - Multiple sclerosis
KW  - Polymorphism, single nucleotide
KW  - Quantitative trait loci
TI  - Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis.
TY  - research article
VL  - 31
ER  -