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Dexamethasone, a direct modulator of AQP2 in Menière's disease | bioRxiv
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
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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Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects | Brazilian Journal of Otorhinolaryngology
Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome | Nature Communications
Distribution of Type IV Collagen in the Cochlea in Alport Syndrome
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Frontiers | Prognostic Gene Expression Signature for Age-Related Hearing Loss
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Clinical Problems of Congenital and Perinatal Cytomegalovirus (CMV) Infection | ARC Journal of Pediatrics
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 - ScienceDirect
Indispensable Role of Ion Channels and Transporters in the Auditory System - Mittal - 2017 - Journal of Cellular Physiology - Wiley Online Library
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
IJMS | Free Full-Text | Genetic Mechanism Study of Auditory Phoenix Spheres and Transcription Factors Prediction for Direct Reprogramming by Bioinformatics
PDF) CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family
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
PDF) CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family