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GEMINs: potential therapeutic targets for spinal muscular atrophy?
The motor neuron degenerative disease spinal muscular atrophy (SMA) remains one of the most frequently inherited causes of infant mortality. Afflicted patients loose the survival motor neuron 1 (SMN1) gene but retain one or more copies of SMN2, a homolog that is incorrectly spliced. Primary treatmen...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4197776/ https://ncbi.nlm.nih.gov/pubmed/25360080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2014.00325 |
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