Adduru, Mhy-Lanie

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

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

Circulation: Genomic and Precision Medicine | April 21, 2025 | Volume: 18 | Issue: 3 | Pages: No page available

10.1161/circgen.124.004976