Items where Author is "Sepehrnejad, Mahsa"
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Number of items: 3.
(2020) A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Bmc Medical Genetics.
(2017) Beck Depression Inventory-II in Hearing Impaired Elderly Patients: A Presbycusis Study. Indian Journal of Otology. pp. 168-170. ISSN 0971-7749
(2017) Evaluation of ophthalmic disorders in children with congenital Sensorineural hearing loss and cochlear implant. Journal of Isfahan Medical School. pp. 1006-1012. ISSN 10277595 (ISSN)