Compound heterozygous variants of the SLC26A4 gene in a Chinese family with enlarged vestibular aqueducts
Abstract Background To investigate the genetic causes of hearing loss in patients with enlarged vestibular aqueduct (EVA), the SLC26A4-related genotypes and phenotypes were analyzed. SLC26A4 gene is closely associated with EVA and its homozygous mutations or compound heterozygous mutations may cause...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2022-07-01T00:00:00Z.
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