טוען...
Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
Spinal muscular atrophy (SMA), the most common autosomal recessive neurodegenerative disease affecting children, results in impaired motor neuron function1. Despite knowledge of the pathogenic role of decreased survival motor neuron (SMN) protein levels, efforts to increase SMN have not resulted in...
שמור ב:
| Main Authors: | , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2010
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2889698/ https://ncbi.nlm.nih.gov/pubmed/20190738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nbt.1610 |
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