Mitochondrial disease in childhood
Mitochondrial disease is the most commonly inherited neurometabolic disease in childhood with an estimated birth prevalence of 1 in 7634. This heterogeneous disease group can be caused by primary mitochondrial DNA mutations or secondary to nuclear gene mutations and have a variable disease onset and...
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University of Newcastle upon Tyne
2015
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.722579 |