A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss
Abstract Background Autosomal recessive non-syndromic hearing loss (ARNSHL) is genetically and phenotypically heterogeneous with over 110 genes causally implicated in syndromic and non-syndromic hearing loss. Here, we investigate the genetic etiology of deafness in two GJB2 and GJB6 negative patient...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
BMC,
2021-02-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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