Report of rare and novel mutations in candidate genes in a cohort of hearing‐impaired patients
Author:
Affiliation:
1. Department of Otorhinolaryngology, The First Affiliated Hospital Sun Yat‐sen University and Institute of Otorhinolaryngology, Sun Yat‐sen University Guangzhou China
Funder
Young Teacher Foundation of Sun Yat-sen University
Guangdong Science and Technology Department
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1887
Reference31 articles.
1. Study of USH1 Splicing Variants through Minigenes and Transcript Analysis from Nasal Epithelial Cells
2. Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum
3. Mutations in the OTOF Gene in Taiwanese Patients with Auditory Neuropathy
4. Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
5. Hearing loss prevalence and years lived with disability, 1990–2019: findings from the Global Burden of Disease Study 2019
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