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  1. Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss

    Article • Fetal and Pediatric Pathology, December 2018, Taylor & Francis

    Mahsa Farjami, Sima Mansoori Derakhshan, maliheh alimardani