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ORIGINAL ARTICLE

Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot

Kheirollahi Majid, Khosravi Fereshteh, Ashouri Saeideh, Ahmadi Alireza

Year : 2016| Volume: 21| Issue : 1 | Page no: 24-24

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2 Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease
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3 Ultrastructural features of cardiomyocytes in infants with tetralogy of Fallot in the first year of life
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