A novel variant in a Chinese couple with hearing loss
Objective To perform molecular diagnosis and genetic counseling in a young Chinese couple with congenital hearing loss. Methods Variant screening analysis was performed by PCR and direct Sanger sequencing or targeted next-generation sequencing of all known hearing loss genes. Novel variants were eva...
Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2019-12-01
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Series: | Journal of International Medical Research |
Online Access: | https://doi.org/10.1177/0300060519884197 |