Items where Author is "Yazdanpanahi, N."

(2019) DNMT3B-579G > T (rs1569686G > T) polymorphism and the risk of multiple sclerosis in a subset of Iranian population. Iranian Journal of Neurology. pp. 70-75. ISSN 2008-384X

(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) Investigation of ERG Gene Expression in Iranian Patients with Multiple Sclerosis. Immunological Investigations. pp. 351-359. ISSN 0882-0139

(2018) RAD51 135G > C polymorphism and risk of sporadic colorectal cancer in Iranian population. Journal of Cancer Research and Therapeutics. pp. 614-618. ISSN 0973-1482

(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) 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