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The C9orf72-SMCR8-WDR41 complex is a GAP for small GTPases
Massive expansions of the hexanucleotide in C9orf72 are the primary genetic origins of familial amyotrophic lateral sclerosis (ALS) and frontal temporal dementia (FTD). Current studies have found that this repeat sequence participates in the disease process by producing neurotoxic substances and red...
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| Gepubliceerd in: | Autophagy |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Taylor & Francis
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7469575/ https://ncbi.nlm.nih.gov/pubmed/32521185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15548627.2020.1779473 |
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