Associated Papers
Genetic architecture of hypertrophic cardiomyopathy in individuals of Chinese and United Kingdom ancestry.
Wang J et al.
Precision Clinical Medicine, 2025
40860236 (PubMed )
Supplement: pbaf019_supplemental_files.zip › Supplemental_Tables.pdf
An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamten.
Leinhos L et al.
Scientific Reports, 2025
40128237 (PubMed )
Supplement: 41598_2025_94371_MOESM1_ESM.pdf
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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