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Title:	RNA metabolism and the pathogenesis of motor neuron diseases
Source:	Trends in Neurosciences [0166-2236] Lemmens, Robin yr:2010

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description	19.	Carlson, K. "Emerging pathogenic pathways in the spinocerebellar ataxias." Current opinion in genetics & development 19.3 (2009): 247-253.
description	20.	Weinberg, Marc S S. "Short non-coding RNA biology and neurodegenerative disorders: novel disease targets and therapeutics." Human Molecular Genetics 18.R1 (2009): -39.