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. - EL Bouchikhi, Ihssane; Belhassan, Khadija; Moufid, Fatima Zohra; Bouguenouch, Laila; Samri, Imane; Iraqui Houssaïni, Mohammed; Ouldim, Karim; Atmani, Samir (Egyptian Journal of Medical Human Genetics, 2021)