J, K., B, K., A, G., AB, A., B, A., S, T., & BP, M. (2025). Beyond the homozygous paradigm: Symptomatic partial biotinidase deficiency in a heterozygous child-first case report from Nepal. BMC pediatrics, 25(1), 450. https://doi.org/10.1186/s12887-025-05822-2
Chicago Style (17th ed.) CitationJ, Kunwar, Kunwar B, Ghimire A, Adhikari AB, Aryal B, Thapa S, and Manandhar BP. "Beyond the Homozygous Paradigm: Symptomatic Partial Biotinidase Deficiency in a Heterozygous Child-first Case Report from Nepal." BMC Pediatrics 25, no. 1 (2025): 450. https://doi.org/10.1186/s12887-025-05822-2.
MLA (9th ed.) CitationJ, Kunwar, et al. "Beyond the Homozygous Paradigm: Symptomatic Partial Biotinidase Deficiency in a Heterozygous Child-first Case Report from Nepal." BMC Pediatrics, vol. 25, no. 1, 2025, p. 450, https://doi.org/10.1186/s12887-025-05822-2.