Items where Author is "Farrokhi, E."

Article

(2023) Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study. Journal of Biomolecular Structure & Dynamics. pp. 9850-9864. ISSN 1538-0254 (Electronic) 0739-1102 (Linking)

(2023) New molecular insights into the A218V variant impact on the steroidogenic acute regulatory protein (STAR) associated with 46, XY disorders of sexual development. Molecular Genetics and Genomics. pp. 693-708. ISSN 1617-4615

(2019) Mutation Analysis of GJB2 and GJB6 Genes and Screening of Nine Common DFNB Loci in Iranian Pedigrees with Autosomal Recessive Nonsyndromic Hearing Loss. Indian Journal of Otology. pp. 97-102. ISSN 0971-7749

(2019) Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran. Journal of Audiology and Otology. pp. 20-26. ISSN 2384-1621

(2018) A novel variant of SLC26A4 and first report of the c.716T > A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss. American Journal of Otolaryngology. pp. 719-725. ISSN 0196-0709

(2015) Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells. Iranian biomedical journal. pp. 160-4. ISSN 2008-823X (Electronic) 1028-852X (Linking)

(2015) The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness. International Journal of Audiology. pp. 124-130. ISSN 1499-2027