P4.60 Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation von Tuppen, H.A.L, Fehmi, J, Czermin, B, Goffrini, P, Meloni, F, Ferrero, I, He, L, Blakely, E.L, McFarland, R, Horvath, R, Turnbull, D.M, Taylor, R.W

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P75 Infantile reversible COX deficiency myopathy caused by the m.14674T>C mutation in mt-tRNAGlu in a German family von Horvath, R, Kemp, J.P, Tuppen, H.A.L, Hudson, G, Pyle, A, Holinski-Feder, E, Abicht, A, Czermin, B, Walter, M.C, Günther-Scholz, A, Smith, P.M, McFarland, R, Chrzanowska-Lightowlers, Z.M.A, Lightowlers, R.N, Lochmüller, H, Taylor, R.W, Chinnery, P.F

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P75 Infantile reversible COX deficiency myopathy caused by the m.14674T>C mutation in mt-tRNA Glu in a German family von Horvath, R., Kemp, J.P., Tuppen, H.A.L., Hudson, G., Pyle, A., Holinski-Feder, E., Abicht, A., Czermin, B., Walter, M.C., Günther-Scholz, A., Smith, P.M., McFarland, R., Chrzanowska-Lightowlers, Z.M.A., Lightowlers, R.N., Lochmüller, H., Taylor, R.W., Chinnery, P.F.

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