Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis

The underlying dataset has been published as supplementary material of the article in the publisher platform at DOI 10.1093/hmg/ddac009

Detalles Bibliográficos
Autores:	Alcina, Antonio, Fedetz, María, Vidal-Cobo, Isabel, Andrés-León, Eduardo, García-Sánchez, María Isabel, Barroso del Jesús, Alicia, Eichau, Sara, Gil-Varea, Elia, Villar, Luisa M., Sáiz, Albert, Leyva, Laura, Vandenbroeck, Koen, Otaegui, David, Gea-Izquierdo, Guillermo, Comabella, Manuel, Urcelay, Elena, Matesanz, Fuencisla
Tipo de recurso:	artículo
Estado:	Versión publicada
Fecha de publicación:	2022
País:	España
Institución:	Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:	DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:	oai:digital.csic.es:10261/378203
Acceso en línea:	http://hdl.handle.net/10261/378203 https://api.elsevier.com/content/abstract/scopus_id/85127885036
Access Level:	acceso abierto
Palabra clave:	Transcription Genetic Central nervous system Demyelinating diseases Carrier proteins Codon Initiator Genes Genome Genotype Introns Multiple sclerosis Single nucleotide polymorphism Protein isoforms Recombination Immunoglobulins Genetics Rna Notch signaling pathway Genome-wide association study Quantitative trait loci Rna-seq

Descripción
Sumario:	The underlying dataset has been published as supplementary material of the article in the publisher platform at DOI 10.1093/hmg/ddac009