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Coilin forms the bridge between Cajal bodies and SMN, the Spinal Muscular Atrophy protein
Spinal muscular atrophy (SMA) is a genetic disorder caused by mutations in the human survival of motor neuron 1 gene, SMN1. SMN protein is part of a large complex that is required for biogenesis of various small nuclear ribonucleoproteins (snRNPs). Here, we report that SMN interacts directly with th...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC312817/ https://ncbi.nlm.nih.gov/pubmed/11641277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.908401 |
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