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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...
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| Publicado no: | Front Cell Dev Biol |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6369352/ https://ncbi.nlm.nih.gov/pubmed/30778386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2019.00007 |
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