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Dysregulation of BMP, Wnt, and Insulin Signaling in Fragile X Syndrome
Drosophila models of neurological disease contribute tremendously to research progress due to the high conservation of human disease genes, the powerful and sophisticated genetic toolkit, and the rapid generation time. Fragile X syndrome (FXS) is the most prevalent heritable cause of intellectual di...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307498/ https://www.ncbi.nlm.nih.gov/pubmed/35880195 http://dx.doi.org/10.3389/fcell.2022.934662 |