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(2023) Novel missense mutation in NKX2.6 gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease. Gene Reports.
(2020) Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients. Applied biochemistry and biotechnology. pp. 896-906. ISSN 1559-0291
(2020) Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease. Applied biochemistry and biotechnology. ISSN 1559-0291
(2018) Polymorphisms of sperm protamine genes and CMA3 staining in infertile men with varicocele. Revista internacional de andrologia. ISSN 1698-0409
(2018) Novel Point Mutations in the Gene in Pediatric Patients with Non-Familial Congenital Heart Disease. Medicina (Kaunas, Lithuania). ISSN 1648-9144
(2016) A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome. Archives of Iranian medicine. pp. 403-8. ISSN 1735-3947
(2016) Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients. Research in cardiovascular medicine. e29134. ISSN 2251-9572