A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
Abstract Background Childhood hearing impairment (HI) is genetically heterogeneous with many implicated genes, however, only a few of these genes are reported in African populations. Methods This study used exome and Sanger sequencing to resolve the possible genetic cause of non-syndromic HI in a Gh...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2022-11-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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