Associated Papers
Unraveling the cellular characteristics of cardiomyopathy with rare variant-driven gene signatures using multi-omics analysis.
Jeong HE et al.
Scientific Reports, 2025
41469780 (PubMed )
Supplement: 41598_2025_33901_MOESM8_ESM.xlsx › TableS1
High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients.
Ryu SW et al.
Frontiers in Cardiovascular Medicine, 2024
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