Recurrent myoglobinuria and deranged acylcarnitines due to a mutation in the mtDNA MT-CO2 gene von Vissing, Christoffer Rasmus, Duno, Morten, Olesen, Jess Have, Rafiq, Jabin, Risom, Lotte, Christensen, Ernst, Wibrand, Flemming, Vissing, John

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A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood von Born, Alfred Peter, Duno, Morten, Rafiq, Jabin, Risom, Lotte, Wibrand, Flemming, Østergaard, Elsebet, Vissing, John

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A mitochondrial tRNA super(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood von Born, Alfred Peter, Duno, Morten, Rafiq, Jabin, Risom, Lotte, Wibrand, Flemming, Oestergaard, Elsebet, Vissing, John

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A mitochondrial tRNAMet mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood von Born, Alfred Peter, Duno, Morten, Rafiq, Jabin, Risom, Lotte, Wibrand, Flemming, Østergaard, Elsebet, Vissing, John

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A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>A associated with pure myopathy von Jeppesen, Tina Dysgaard, Duno, Morten, Risom, Lotte, Wibrand, Flemming, Rafiq, Jabin, Krag, Thomas, Jakobsen, Johannes, Andersen, Henning, Vissing, John

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Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation von Rafiq, Jabin, Duno, Morten, Østergaard, Elsebet, Ravn, Kirstine, Vissing, Christoffer R., Wibrand, Flemming, Vissing, John

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