P75 Infantile reversible COX deficiency myopathy caused by the m.14674T>C mutation in mt-tRNAGlu in a German family
Titel:
P75 Infantile reversible COX deficiency myopathy caused by the m.14674T>C mutation in mt-tRNAGlu in a German family
Auteur:
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.