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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 - ScienceDirect
Biomolecules | Free Full-Text | Linking Cerebrovascular Dysfunction to Age-Related Hearing Loss and Alzheimer’s Disease—Are Systemic Approaches for Diagnosis and Therapy Required?
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
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
Clinical Problems of Congenital and Perinatal Cytomegalovirus (CMV) Infection | ARC Journal of Pediatrics
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IJMS | Free Full-Text | Genetic Mechanism Study of Auditory Phoenix Spheres and Transcription Factors Prediction for Direct Reprogramming by Bioinformatics
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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
Dexamethasone, a direct modulator of AQP2 in Menière's disease | bioRxiv
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
Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome | Nature Communications
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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