Clinical validity of autosomal dominant ALPK3 loss-of-function variants as a cause of hypertrophic cardiomyopathy

Sophie Hespe, Emma S Singer, Chloe Reuter, Brittney Murray, Elizabeth Jordan, Jessica Chowns, Stacey Peters, Megan Mayers, Belinda Gray, Ray E Hershberger, Anjali T Owens, Christopher Semsarian, Amber Waddell, Babken Asatryan, Emma Owens, Courtney Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily E Brown, Lily Hoffman-Andrews, Fergus Stafford, Richard D Bagnall, Lucas Bronicki, Bert Callewaert, C Anwar A Chahal, Cynthia James, Olga Jarinova, Andrew P Landstrom, Elizabeth M McNally, Laura Muiño-Mosquera, Victoria Parikh, Roddy Walsh, Bess Wayburn, James S. Ware, Benjamin L Parker, Enzo R Porrello, David A Elliott, James W McNamara, Jodie Ingles