Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy

Circ Genom Precis Med. 2025 Jun;18(3):e004976. doi: 10.1161/CIRCGEN.124.004976. Epub 2025 Apr 21.
No abstract available

Keywords: cardiomyopathy, hypertrophic; exons; myocytes, cardiac; phenotype; protein kinases.

Publication types

  • Letter