IJMS | Free Full-Text | Genetic Mechanism Study of Auditory Phoenix Spheres and Transcription Factors Prediction for Direct Reprogramming by Bioinformatics
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PDF) A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
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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
Whole exome sequencing identified a second pathogenic variant in HOMER2 for autosomal dominant non‐syndromic deafness - Lu - 2018 - Clinical Genetics - Wiley Online Library
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Temporal Bone Histopathology in Alport Syndrome
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