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SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain
Spinal muscular atrophy (SMA) is a recessive neuromuscular disease caused by mutations in the human survival motor neuron 1 (SMN1) gene. The human SMN protein is part of a large macromolecular complex involved in the biogenesis of small ribonucleoproteins. Previously, we showed that SMN is a sarcome...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2566527/ https://ncbi.nlm.nih.gov/pubmed/18689355 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn234 |
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