Cite
Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease-causing variants.
MLA
Sadat Fatemi, Seyedeh Helia, et al. “Genetic Evaluation of Hyperphenylalaninemia Patients with Tetrahydrobiopterin Deficiency in Iranian Population: Identification of Four Novel Disease-Causing Variants.” Molecular Genetics & Genomic Medicine, vol. 10, no. 12, Dec. 2022, p. e2081. EBSCOhost, https://doi.org/10.1002/mgg3.2081.
APA
Sadat Fatemi, S. H., Eshraghi, P., Ghanei, M., & Hamzehloei, T. (2022). Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease-causing variants. Molecular Genetics & Genomic Medicine, 10(12), e2081. https://doi.org/10.1002/mgg3.2081
Chicago
Sadat Fatemi, Seyedeh Helia, Peyman Eshraghi, Mahmoud Ghanei, and Tayebeh Hamzehloei. 2022. “Genetic Evaluation of Hyperphenylalaninemia Patients with Tetrahydrobiopterin Deficiency in Iranian Population: Identification of Four Novel Disease-Causing Variants.” Molecular Genetics & Genomic Medicine 10 (12): e2081. doi:10.1002/mgg3.2081.