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The KHENEREXT Study
mitochondrial diseases, mitochondrial dna trnaleu(uur) m.3243a<g mutation, maternally inherited diabetes and deafness (midd), mitochondrial encephalomyopathy, lactic acidosis and stroke like episodes (melas), chronic progressive external ophthalmoplegia (cpeo), kh176, open label extension, melas, midd, cpeo, oxidative phosphorylation (oxphos), interventional
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