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Integrated genetic and structural analysis reveals HLA-associated celiac disease risk in a Sardinian population, suggesting new interpretative frameworks.
By integrating genetic and in silico structural analyses, this study highlights that HLA-associated susceptibility to celiac disease reflects not only allele and haplotype distribution but also subtle, allele-specific features in the structural organization of peptide-binding regions. These findings provide a refined framework for interpreting HLA-DQ-mediated genetic risk and support the relevance of structural coherence as a complementary dimension in the assessment of disease susceptibility.
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Cannea et al. (2026) studied this question.
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