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The ALS/FTLD associated protein C9orf72 associates with SMCR8 and WDR41 to regulate the autophagy-lysosome pathway
Hexanucleotide repeat expansion in the C9orf72 gene is a leading cause of frontotemporal lobar degeneration (FTLD) with amyotrophic lateral sclerosis (ALS). Reduced expression of C9orf72 has been proposed as a possible disease mechanism. However, the cellular function of C9orf72 remains to be charac...
Autores principales: | Sullivan, Peter M., Zhou, Xiaolai, Robins, Adam M., Paushter, Daniel H., Kim, Dongsung, Smolka, Marcus B., Hu, Fenghua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870812/ https://www.ncbi.nlm.nih.gov/pubmed/27193190 http://dx.doi.org/10.1186/s40478-016-0324-5 |
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