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The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy

Spinal muscular atrophy (SMA), which is caused by inactivating mutations in the survival motor neuron 1 (SMN1) gene, is characterized by loss of lower motor neurons in the spinal cord. The gene encoding SMN is very highly conserved in evolution, allowing the disease to be modeled in a range of speci...

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Detaylı Bibliyografya
Asıl Yazarlar: Sleigh, James N., Gillingwater, Thomas H., Talbot, Kevin
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Company of Biologists Limited 2011
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3124050/
https://ncbi.nlm.nih.gov/pubmed/21708901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.007245
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