No evidence of association of the rare nsSNP rs35667974 in IFIH1 with multiple sclerosis
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,Immunology,Immunology and Allergy
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1. Functional significance of the rare rs35667974 IFIH1 gene polymorphism, associated with multiple autoimmune diseases, using a structural biological approach;Autoimmunity;2022-08-02
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3. RIG-I-Like Receptors and Type I Interferonopathies;Journal of Interferon & Cytokine Research;2017-05
4. Analysis of polymorphisms in RIG-I-like receptor genes in German multiple sclerosis patients;Journal of Neuroimmunology;2014-12
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