APA (7th ed.) Citation

HW, C., H, K., JM, K., DM, S., OH, K., M, Y., . . . MH, P. (2025). Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: A familial analysis revealing oligogenic contributors to disease severity. Orphanet journal of rare diseases, 20(1), 349. https://doi.org/10.1186/s13023-025-03871-5

Chicago Style (17th ed.) Citation

HW, Cho, et al. "Identification of Novel MYO19 Variants in Neonatal Hypertrophic Cardiomyopathy: A Familial Analysis Revealing Oligogenic Contributors to Disease Severity." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 349. https://doi.org/10.1186/s13023-025-03871-5.

MLA (9th ed.) Citation

HW, Cho, et al. "Identification of Novel MYO19 Variants in Neonatal Hypertrophic Cardiomyopathy: A Familial Analysis Revealing Oligogenic Contributors to Disease Severity." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 349, https://doi.org/10.1186/s13023-025-03871-5.