Associated Papers
Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease.
Mansour H et al.
Frontiers in Pediatrics, 2022
A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome.
Oud MM et al.
Cilia, 2016
27069622 (PubMed )
Supplement: 13630_2016_29_MOESM1_ESM.xls › Total_variants
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