APA (7th ed.) Citation

MAM, Y., SM, E., KI, E., SA, T., HSM, A., & MM, E. (2025). Acid β-glucosidase (GBA1) gene mutational spectrum and clinical phenotypes in patients with gaucher disease: Seven novel mutations in a multicenter retrospective cohort study from upper Egypt. Molecular and cellular pediatrics, 12(1), 14. https://doi.org/10.1186/s40348-025-00200-5

Chicago Style (17th ed.) Citation

MAM, Youssef, Elsayed SM, Elsayh KI, Taha SA, Abdelmotogaly HSM, and Embaby MM. "Acid β-glucosidase (GBA1) Gene Mutational Spectrum and Clinical Phenotypes in Patients with Gaucher Disease: Seven Novel Mutations in a Multicenter Retrospective Cohort Study from Upper Egypt." Molecular and Cellular Pediatrics 12, no. 1 (2025): 14. https://doi.org/10.1186/s40348-025-00200-5.

MLA (9th ed.) Citation

MAM, Youssef, et al. "Acid β-glucosidase (GBA1) Gene Mutational Spectrum and Clinical Phenotypes in Patients with Gaucher Disease: Seven Novel Mutations in a Multicenter Retrospective Cohort Study from Upper Egypt." Molecular and Cellular Pediatrics, vol. 12, no. 1, 2025, p. 14, https://doi.org/10.1186/s40348-025-00200-5.