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...
שמור ב:
| הוצא לאור ב: | EMBO J |
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| Principais autores: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Nature Publishing Group
2001
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC125643/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11574476/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/20.19.5443 |
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