Reduced survival of motor neuron (SMN) protein in motor neuronal progenitors functions cell autonomously to cause spinal muscular atrophy in model mice expressing the human centromeric (SMN2) gene.

Source:http://linkedlifedata.com/resource/pubmed/id/20826664

J. Neurosci. 2010 Sep 8 30 36 12005-19

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20826664