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Identification of CDC42 Effectors Operating in FGD1-Dependent Trafficking at the Golgi
Loss of function mutations in the FGD1 gene cause a rare X-linked disease, faciogenital dysplasia (FGDY, also known as Aarskog-Skott syndrome), which is associated with bone and urogenital abnormalities. The FGD1 gene encodes à CDC42-specific guanine nucleotide exchange factor. The mutations are fre...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369352/ https://www.ncbi.nlm.nih.gov/pubmed/30778386 http://dx.doi.org/10.3389/fcell.2019.00007 |