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RNA-recognition motif in Matrin-3 mediates neurodegeneration through interaction with hnRNPM
BACKGROUND: Amyotrophic lateral sclerosis (ALS) is an adult-onset, fatal neurodegenerative disease characterized by progressive loss of upper and lower motor neurons. While pathogenic mutations in the DNA/RNA-binding protein Matrin-3 (MATR3) are linked to ALS and distal myopathy, the molecular mecha...
Autores principales: | Ramesh, Nandini, Kour, Sukhleen, Anderson, Eric N., Rajasundaram, Dhivyaa, Pandey, Udai Bhan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437177/ https://www.ncbi.nlm.nih.gov/pubmed/32811564 http://dx.doi.org/10.1186/s40478-020-01021-5 |
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