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<title>Medical Xpress: PHYSorg news tagged with: neuromuscular diseases</title>
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     <title>Researchers generate mutant mouse model useful in treatment of neuromuscular diseases</title>
   	 <description>Researchers at the University of Granada have produced for the first time in the world mice lacking the coenzyme Q10, a rare mitochondrial disease prevailingly affecting children. The researchers needed three years to complete the study.</description>
     <link>http://medicalxpress.com/news/2013-01-mutant-mouse-treatment-neuromuscular-diseases.html</link>
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	 <pubDate>Tue, 29 Jan 2013 10:22:30 EST</pubDate>
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     <title>Study finds how to correct human mitochondrial mutations</title>
   	 <description>Researchers at the UCLA stem cell center and the departments of chemistry and biochemistry and pathology and laboratory medicine have identified, for the first time, a generic way to correct mutations in human mitochondrial DNA by targeting corrective RNAs, a finding with implications for treating a host of mitochondrial diseases.</description>
     <link>http://medicalxpress.com/news/2012-03-human-mitochondrial-mutations.html</link>
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	 <pubDate>Mon, 12 Mar 2012 15:00:03 EST</pubDate>
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     <title>Unusual alliances enable movement</title>
   	 <description>Some unusual alliances are necessary for you to wiggle your fingers, researchers report.</description>
     <link>http://medicalxpress.com/news/2012-02-unusual-alliances-enable-movement.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 08 Feb 2012 10:45:58 EST</pubDate>
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