Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum

Anti- C N1A antibodies in South Australian patients with inclusion body myositis

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LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants: Fig. 1.

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Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes

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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

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188th ENMC International Workshop: Inclusion Body Myositis, 2–4 December 2011, Naarden, The Netherlands

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Autoantibodies to cytosolic 5′-nucleotidase 1A in inclusion body myositis

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Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis

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Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis

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Inclusion body myositis

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