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Characterizing Motor Neuron-specific mRNA Processing Defects in an Intermediate Mouse Model of Spinal Muscular Atrophy
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Axonal transport of spinal muscular atrophy (SMA) disease protein
survival of motor neuron (SMN) and rescue of axonal defects by the
mRNA-binding proteins IMP1 and HuD
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SMN functions as a molecular chaperone for mRNP assembly
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