Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility

CONTEXT: A recent large-scale analysis of non-synonymous coding polymorphisms showed strong evidence that an alanine to threonine amino acid change at codon 946 of the interferon-induced helicase (IFIH1) gene (SNP ID rs1990760) was associated with type 1 diabetes. Previous investigations have also d...

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Detalhes bibliográficos
Publicado no:J Clin Endocrinol Metab
Main Authors: Sutherland, Alison, Davies, Jocelyn, Owen, Catherine J, Vaikkakara, Suresh, Walker, Christine, Cheetham, Timothy D, James, R Andrew, Perros, Petros, Donaldson, Peter T, Cordell, Heather J, Quinton, Richard, Pearce, Simon HS
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6952273/
https://ncbi.nlm.nih.gov/pubmed/17535987
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2007-0173
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