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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 SMPX gene and the loss of function has been suggested as the underlying mechanism. In the attempt to confirm this hypothesis we generated an Smpx-d...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235540/ https://www.ncbi.nlm.nih.gov/pubmed/34204426 http://dx.doi.org/10.3390/ijms22126497 |