Inner Ear and Muscle Developmental Defects in Smpx-Deficient Zebrafish Embryos
The last decade has witnessed the identification of several families affected by hereditary non-syndromic hearing loss (NSHL) caused by mutations in the <i>SMPX</i> gene and the loss of function has been suggested as the underlying mechanism. In the attempt to confirm this hypothesis we...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2021-06-01
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| Series: | International Journal of Molecular Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1422-0067/22/12/6497 |