Disruption of pathways regulated by Integrator complex in Galloway–Mowat syndrome due to WDR73 mutations

Several studies have reported WDR73 mutations to be causative of Galloway–Mowat syndrome, a rare disorder characterised by the association of neurological defects and renal-glomerular disease. In this study, we demonstrate interaction of WDR73 with the INTS9 and INTS11 components of Integrator, a la...

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Detalles Bibliográficos
Autores principales: Tilley, F. C., Arrondel, C., Chhuon, C., Boisson, M., Cagnard, N., Parisot, M., Menara, G., Lefort, N., Guerrera, I. C., Bole-Feysot, C., Benmerah, A., Antignac, C., Mollet, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940485/
https://www.ncbi.nlm.nih.gov/pubmed/33686175
http://dx.doi.org/10.1038/s41598-021-84472-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940485/
https://www.ncbi.nlm.nih.gov/pubmed/33686175
http://dx.doi.org/10.1038/s41598-021-84472-7

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