EL Bouchikhi, I., Belhassan, K., Moufid, F. Z., Bouguenouch, L., Samri, I., Iraqui Houssaïni, M., . . . Atmani, S. (2021). Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: Worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype. Egyptian Journal of Medical Human Genetics, 22(1), 1. https://doi.org/10.1186/s43042-021-00136-1
Chicago Style (17th ed.) CitationEL Bouchikhi, Ihssane, Khadija Belhassan, Fatima Zohra Moufid, Laila Bouguenouch, Imane Samri, Mohammed Iraqui Houssaïni, Karim Ouldim, and Samir Atmani. "Screening of NKX2.5 Gene in Moroccan Tetralogy of Fallot (TOF) Patients: Worldwide Mutation Rate Comparisons Show a Significant Association Between R25C Variant and TOF Phenotype." Egyptian Journal of Medical Human Genetics 22, no. 1 (2021): 1. https://doi.org/10.1186/s43042-021-00136-1.
MLA (9th ed.) CitationEL Bouchikhi, Ihssane, et al. "Screening of NKX2.5 Gene in Moroccan Tetralogy of Fallot (TOF) Patients: Worldwide Mutation Rate Comparisons Show a Significant Association Between R25C Variant and TOF Phenotype." Egyptian Journal of Medical Human Genetics, vol. 22, no. 1, 2021, p. 1, https://doi.org/10.1186/s43042-021-00136-1.
