Report of rare and novel mutations in candidate genes in a cohort of hearing‐impaired patients
Abstract Background Many hearing‐impaired patients carry mutations in rare or novel genes undetected in regular genetic hot regions/genes screening. Methods We collected clinical and genetic data from subjects with hearing loss who visited our department for genetic counseling. Next‐generation seque...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2022-04-01
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| Series: | Molecular Genetics & Genomic Medicine |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/mgg3.1887 |