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Spinal muscular atrophy: the role of SMN in axonal mRNA regulation
Spinal muscular atrophy (SMA) is a neurodegenerative disease caused by homozygous mutations or deletions in the survival of motor neuron (SMN1) gene, encoding the ubiquitously expressed SMN protein. SMN associates with different proteins (Gemins 2-8, Unrip) to form a multimeric complex involved in t...
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| Huvudupphovsmän: | , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2012
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3360984/ https://ncbi.nlm.nih.gov/pubmed/22330725 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2012.01.044 |
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