about
PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data.The individual or combinational effects of Hesperetin and Letrozole on the activity and expression of aromatase in MCF-7 cells.Simple renal cysts and hypertension are associated with angiotensinogen (AGT) gene variant in Shiraz population (Iran).A Novel Variant in the PAH Gene Causing Phenylketonuria in an Iranian PedigreeAn Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene.Association between HIC1 and RASSF1A promoter hypermethylation with MTHFD1 G1958A polymorphism and clinicopathological features of breast cancer in Iranian patients.Incidence of human herpes virus-6 and human cytomegalovirus infections in donated bone marrow and umbilical cord blood hematopoietic stem cells.Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes.Genetic analysis of Iranian autosomal dominant polycystic kidney disease: new insight to haplotype analysis.Human herpesvirus-6 viral load and antibody titer in serum samples of patients with multiple sclerosis.Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation
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researcher ORCID ID = 0000-0002-2608-464X
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0000-0002-2608-464X