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- W1613556889 abstract "Spinal muscular atrophy (SMA) is the most common genetic neurodegenerative disease leading to death in childhood. SMA is characterized by the loss of spinal cord anterior horn neurons and progressive denervation of skeletal muscles. SMA is caused by deletion or mutation of the telomeric copy of human survival motor neuron gene 1 (hSMN1) and retention of the hSMN2 gene. SMA animal models are extremely useful in studying the mechanism of SMA-related motoneuronal death, and may provide an in vivo system for testing a potential SMA therapy. doi : 10.5214/ans.0972.7531.1118407" @default.
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- W1613556889 date "2011-08-19" @default.
- W1613556889 modified "2023-09-27" @default.
- W1613556889 title "Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms" @default.
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- W1613556889 doi "https://doi.org/10.5214/ans.0972.7531.1118407" @default.
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