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Functional characterization of SMN evolution in mouse models of SMA

Spinal Muscular Atrophy (SMA) is a monogenic neurodegenerative disorder and the leading genetic cause of infantile mortality. While several functions have been ascribed to the SMN (survival motor neuron) protein, their specific contribution to the disease has yet to be fully elucidated. We hypothesi...

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Udgivet i:Sci Rep
Main Authors: Osman, Erkan Y., Bolding, Madeline R., Villalón, Eric, Kaifer, Kevin A., Lorson, Zachary C., Tisdale, Sarah, Hao, Yue, Conant, Gavin C., Pires, J. Chris, Pellizzoni, Livio, Lorson, Christian L.
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group UK 2019
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6603021/
https://ncbi.nlm.nih.gov/pubmed/31263170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-45822-8
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