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Therapy Development for Spinal Muscular Atrophy in SMN Independent Targets

Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder, leading to progressive muscle weakness, atrophy, and sometimes premature death. SMA is caused by mutation or deletion of the survival motor neuron-1 (SMN1) gene. An effective treatment does not presently exist. Since...

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Detalhes bibliográficos
Autor principal: Tsai, Li-Kai
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3369530/
https://ncbi.nlm.nih.gov/pubmed/22701806
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/456478
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