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.

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Bibliographic Details
Title:	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.
Authors:	EL Bouchikhi, Ihssane^1,2 (AUTHOR) ihssane.elbouchikhi@usmba.ac.ma, Belhassan, Khadija¹ (AUTHOR), Moufid, Fatima Zohra¹ (AUTHOR), Bouguenouch, Laila¹ (AUTHOR), Samri, Imane¹ (AUTHOR), Iraqui Houssaïni, Mohammed³ (AUTHOR), Ouldim, Karim¹ (AUTHOR), Atmani, Samir⁴ (AUTHOR)
Source:	Egyptian Journal of Medical Human Genetics. 3/11/2021, Vol. 22 Issue 1, p1-7. 7p.
Database:	Academic Search Ultimate

Description
ISSN:	11108630
DOI:	10.1186/s43042-021-00136-1