APA (7th ed.) Citation

Al Busaidi, M., Mohamed, F. E., Al-Ajmi, E., Al Hashmi, N., Al-Thihli, K., Al Futaisi, A., . . . Al-Jasmi, F. (2023). Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: Novel PCK1 variants in four Arabian Gulf families. Orphanet Journal of Rare Diseases, 18(1), 1. https://doi.org/10.1186/s13023-023-02946-5

Chicago Style (17th ed.) Citation

Al Busaidi, Marwa, Feda E. Mohamed, Eiman Al-Ajmi, Nadia Al Hashmi, Khalid Al-Thihli, Amna Al Futaisi, Watfa Al Mamari, Fathiya Al-Murshedi, and Fatma Al-Jasmi. "Expanding the Clinical Spectrum of Cytosolic Phosphoenolpyruvate Carboxykinase Deficiency: Novel PCK1 Variants in Four Arabian Gulf Families." Orphanet Journal of Rare Diseases 18, no. 1 (2023): 1. https://doi.org/10.1186/s13023-023-02946-5.

MLA (9th ed.) Citation

Al Busaidi, Marwa, et al. "Expanding the Clinical Spectrum of Cytosolic Phosphoenolpyruvate Carboxykinase Deficiency: Novel PCK1 Variants in Four Arabian Gulf Families." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, p. 1, https://doi.org/10.1186/s13023-023-02946-5.