CP, H., JH, T., P, S., A, H., TP, C., IP, H., . . . AA, W. (2026). Z variant heterozygosity in alpha-1 antitrypsin deficiency: Disease risk and treatment implications. Orphanet journal of rare diseases, 21(1), . https://doi.org/10.1186/s13023-026-04283-9
Chicago Style (17th ed.) CitationCP, Hersh, et al. "Z Variant Heterozygosity in Alpha-1 Antitrypsin Deficiency: Disease Risk and Treatment Implications." Orphanet Journal of Rare Diseases 21, no. 1 (2026). https://doi.org/10.1186/s13023-026-04283-9.
MLA (9th ed.) CitationCP, Hersh, et al. "Z Variant Heterozygosity in Alpha-1 Antitrypsin Deficiency: Disease Risk and Treatment Implications." Orphanet Journal of Rare Diseases, vol. 21, no. 1, 2026, https://doi.org/10.1186/s13023-026-04283-9.