Variant rs4149584 (R92Q) of the TNFRSF1A gene in patients with familial multiple sclerosis

Variant rs4149584 (R92Q) of the TNFRSF1A gene in patients with familial multiple sclerosis

Introduction: Genomic studies have identified numerous genetic variants associated with susceptibility to multiple sclerosis (MS); however, each one explains only a small percentage of the risk of developing the disease. These variants are located in genes involved in specific pathways, which suppor...

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Main Authors: U. Gomez-Pinedo, J.A. Matías-Guiu, L. Torre-Fuentes, P. Montero-Escribano, L. Hernández-Lorenzo, V. Pytel, P. Maietta, S. Alvarez, I. Sanclemente-Alamán, L. Moreno-Jimenez, D. Ojeda-Hernandez, N. Villar-Gómez, M.S. Benito-Martin, B. Selma-Calvo, L. Vidorreta-Ballesteros, R. Madrid, J. Matías-Guiu
Format: Article
Language:English
Published: Elsevier España 2025-01-01
Series:Neurología (English Edition)
Subjects:
Esclerosis múltiple familiar
Genética
Células HOG
Mielinización
TNFRSF1A
Secuenciación de exoma completo
Online Access:http://www.sciencedirect.com/science/article/pii/S2173580822000876
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