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SMN interacts with a novel family of hnRNP and spliceosomal proteins
Spinal muscular atrophy (SMA) is a common neurodegenerative disease caused by deletion or loss-of-function mutations of the survival of motor neurons (SMN) protein. SMN is in a complex with several proteins, including Gemin2, Gemin3 and Gemin4, and it plays important roles in small nuclear ribonucle...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC125643/ https://ncbi.nlm.nih.gov/pubmed/11574476 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/20.19.5443 |
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