Associated Papers
Cardiomyopathy-associated and basic residue mutations in myopalladin alter actin binding, bundling, and structural stability.
Arachchige AR et al.
Protein Science : a Publication of the Protein Society, 2026
Age and Sex Differences in the Genetics of Cardiomyopathy.
Akinrinade O et al.
Journal of Cardiovascular Translational Research, 2023
37477868 (PubMed )
Supplement: 12265_2023_10411_MOESM1_ESM.xlsx › Table_S2_All_variants
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy.
Mazzarotto F et al.
Circulation, 2020
31983221 (PubMed )
Supplement: cir-141-387-s002.xlsx › Table_S3
Genetic Etiology for Alcohol-Induced Cardiac Toxicity.
Ware JS et al.
Journal of the American College of Cardiology, 2018
29773157 (PubMed )
Supplement: mmc2.xlsx › Final_VariantList_Rare_ACMonly
iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers.
Wang M et al.
Scientific Reports, 2016
27527004 (PubMed )
Supplement: srep31321-s4.xls › SwissvarFilteredMix
Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.
Meyer T et al.
European Journal of Human Genetics : Ejhg, 2013
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