Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome | Nature Communications
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Academic Outcomes for School-Aged Children With Severe–Profound Hearing Loss and Early Unilateral and Bilateral Cochlear Implants | Journal of Speech, Language, and Hearing Research
Temporal Bone Histopathology in Alport Syndrome
Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain | PLOS ONE
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Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2 in the Auditory System - Mittal - 2016 - Journal of Cellular Physiology - Wiley Online Library
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Frontiers | Prognostic Gene Expression Signature for Age-Related Hearing Loss
Clinical Problems of Congenital and Perinatal Cytomegalovirus (CMV) Infection | ARC Journal of Pediatrics
Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain | PLOS ONE
PDF) CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family
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Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects | Brazilian Journal of Otorhinolaryngology
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PDF) CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family
