Frontiers | Prognostic Gene Expression Signature for Age-Related Hearing Loss
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Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome | Nature Communications
Distribution of Type IV Collagen in the Cochlea in Alport Syndrome
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
Biomolecules | Free Full-Text | Linking Cerebrovascular Dysfunction to Age-Related Hearing Loss and Alzheimer’s Disease—Are Systemic Approaches for Diagnosis and Therapy Required?
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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
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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Clinical Problems of Congenital and Perinatal Cytomegalovirus (CMV) Infection | ARC Journal of Pediatrics
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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
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Schematic representation of the type II collagen trimer with... | Download Scientific Diagram
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
IJMS | Free Full-Text | Genetic Mechanism Study of Auditory Phoenix Spheres and Transcription Factors Prediction for Direct Reprogramming by Bioinformatics
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
