Associated Papers
Select autosomal dominant DFNA11 deafness variants activate Myo7A targeting in epithelial cells.
Acharya P et al.
Journal of Cell Science, 2025
Select autosomal dominant DFNA11 deafness mutations activate Myo7A in epithelial cells.
Acharya P et al.
Biorxiv : the Preprint Server for Biology, 2024
Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.
Han JH et al.
Journal of Clinical Medicine, 2024
38610765 (PubMed )
Supplement: jcm-13-02001-s001.zip › jcm-2913174-supplementary.xlsx › Supplement_Table_S2
Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation.
Rim JH et al.
Human Genetics, 2022
34519870 (PubMed )
Supplement: 439_2021_2367_MOESM1_ESM.pdf
Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains.
Joo SY et al.
Biomedicines, 2022
Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients.
Iwasa YI et al.
Plos One, 2016
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