Associated Papers
Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
Liu Y et al.
Bmc Oral Health, 2024
38280992 (PubMed )
Supplement: 12903_2024_3888_MOESM2_ESM.xls › Supplementary_Table_1
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis.
Zhang W et al.
Orphanet Journal of Rare Diseases, 2022
35668470 (PubMed )
Supplement: 13023_2022_2349_MOESM5_ESM.xlsx › ________
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A et al.
Nature Communications, 2019
31175295 (PubMed )
Supplement: 41467_2019_10482_MOESM8_ESM.xlsx › Supplementary_Data_5
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