Delivery of recombinant follistatin lessens disease severity in a mouse model of spinal muscular atrophy

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Oxford University Press

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Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy mice

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Animal models of spinal muscular atrophy

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Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition

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A mouse model of spinal and bulbar muscular atrophy

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