Associated Papers
Pathogenetic mechanisms of muscle-specific ribosomes in dilated cardiomyopathy.
Murphy MR et al.
Biorxiv : the Preprint Server for Biology, 2025
Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.
Yang Q et al.
Bmc Medical Genomics, 2023
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies.
Lipov A et al.
Nature Cardiovascular Research, 2023
38666070 (PubMed )
Supplement: 44161_2023_346_MOESM3_ESM.xlsx › S1
Compound Heterozygous Missense Variants in RPL3L Genes Associated with Severe Forms of Dilated Cardiomyopathy: A Case Report and Literature Review.
Das BB et al.
Children (basel, Switzerland), 2022
Select a paper to view details