PDF) A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
Distribution of Type IV Collagen in the Cochlea in Alport Syndrome
Indispensable Role of Ion Channels and Transporters in the Auditory System - Mittal - 2017 - Journal of Cellular Physiology - Wiley Online Library
Cryo-Electron Microscopy Structure and Interactions of the Human Cytomegalovirus gHgLgO Trimer with Platelet-Derived Growth Factor Receptor Alpha | mBio
Autosomal Recessive Alport Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
TRIMER SNHL 3,5 KS - Kosilice i Trimeri - OLX.ba
Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects - ScienceDirect
Trimer SNHL 3.8ks Novi neotpakiran
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IJMS | Free Full-Text | Genetic Mechanism Study of Auditory Phoenix Spheres and Transcription Factors Prediction for Direct Reprogramming by Bioinformatics
Evidence for sensorineural hearing loss in two surviving NHPs following... | Download Scientific Diagram
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Whole exome sequencing identified a second pathogenic variant in HOMER2 for autosomal dominant non‐syndromic deafness - Lu - 2018 - Clinical Genetics - Wiley Online Library
Temporal Bone Histopathology in Alport Syndrome
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Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome | Nature Communications
Frontiers | Prognostic Gene Expression Signature for Age-Related Hearing Loss
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
