Associated Papers
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
Barbosa P et al.
Frontiers in Cardiovascular Medicine, 2022
36061567 (PubMed )
Supplement: Table_1.XLSX › Table_S1
Prioritizing causal disease genes using unbiased genomic features.
Deo RC et al.
Genome Biology, 2014
25633252 (PubMed )
Supplement: 13059_2014_534_MOESM48_ESM.xlsx › Sheet1
Select a paper to view details