Hespe, S., Singer, E. S., Reuter, C., Murray, B., Jordan, E., Chowns, J., … Ingles, J. (2025). Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy. Circ Genom Precis Med, 18(3), e004976. https://doi.org/10.1161/CIRCGEN.124.004976

Hespe, Sophie, Emma S. Singer, Chloe Reuter, Brittney Murray, Elizabeth Jordan, Jessica Chowns, Stacey Peters, et al. “Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.” Circ Genom Precis Med 18, no. 3 (June 2025): e004976. https://doi.org/10.1161/CIRCGEN.124.004976.

Hespe S, Singer ES, Reuter C, Murray B, Jordan E, Chowns J, et al. 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.

Hespe, Sophie, et al. “Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.” Circ Genom Precis Med, vol. 18, no. 3, June 2025, p. e004976. Pubmed, doi:10.1161/CIRCGEN.124.004976.

Hespe S, Singer ES, Reuter C, Murray B, Jordan E, Chowns J, Peters S, Mayers M, Gray B, Hershberger RE, Owens AT, Semsarian C, Waddell A, Asatryan B, Owens E, Thaxton C, Adduru M-L, Anderson K, Brown EE, Hoffman-Andrews L, Stafford F, Bagnall RD, Bronicki L, Callewaert B, Chahal CAA, James CA, Jarinova O, Landstrom AP, McNally EM, Muiño-Mosquera L, Parikh V, Walsh R, Wayburn B, Ware JS, Parker BL, Porrello ER, Elliott DA, McNamara JW, Ingles J. 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.