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  1. Development of a cell based system to investigate which Leigh syndrome patients could...

    Mitochondrial diseases are the most common group of inherited metabolic disorders, with a minimum birth prevalence of ~ 1 in 5000. They are an unusually heterogeneous group of diseases, both phenotypically and genetically. To date over 200 genes

    http://iris.ucl.ac.uk/iris/publication/1126349/1

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