Associated Papers
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
Novel PPP1R13L variant expands the phenotype of a rare cardiocutaneous syndrome.
Henry A et al.
Clinical Genetics, 2022
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