Concurrent Newborn Hearing and Genetic Screening in a Multi-Ethnic Population in South China
Hearing loss is a common sensory deficit in humans with intricate genomic landscape and mutational signature. Approximately 1-3 out of 1,000 newborns have hearing loss and up to 60% of these cases have a genetic etiology. In this study, we conducted the concurrent newborn hearing and genetic screeni...
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Format: | Book |
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Frontiers Media S.A.,
2021-11-01T00:00:00Z.
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A1234.567 |
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