Zheng, Z., Peng, W., Lin, Y., Lin, W., & Wang, G. (2025). Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosis. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03723-2
Chicago Style (17th ed.) CitationZheng, Zhenzhu, Weilin Peng, Yiming Lin, Weihua Lin, and Gaoxiong Wang. "Clinical and Genetic Analysis of Four Chinese Patients with Holocarboxylase Synthetase Deficiency and Metabolic Acidosis." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03723-2.
MLA (9th ed.) CitationZheng, Zhenzhu, et al. "Clinical and Genetic Analysis of Four Chinese Patients with Holocarboxylase Synthetase Deficiency and Metabolic Acidosis." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03723-2.