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...

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Detalles Bibliográficos
Autores principales: Ghilardi, Anna, Diana, Alberto, Bacchetta, Renato, Santo, Nadia, Ascagni, Miriam, Prosperi, Laura, Del Giacco, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235540/
https://www.ncbi.nlm.nih.gov/pubmed/34204426
http://dx.doi.org/10.3390/ijms22126497

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