A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy
R Horváth, H Lochmüller, C Scharfe, B H Do, P J Oefner, J Müller-Höcker, B G Schoser, D Pongratz, D P Auer, M Jaksch
Journal of Medical Genetics Oct 2003, 40 (10) 752-757; DOI: 10.1136/jmg.40.10.752