Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation

Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation / D. Ronchi, S. Orcesi, A. Bordoni, F. Fortunato, E. Fassone, M. Rizzuti, A. Cosi, M. Moggio, A. Berardinelli, P. Veggiotti, G.P. Comi. ((Intervento presentato al convegno ICNMD International Congress on Neuromuscular Disorders 2010 tenutosi a napoli nel 2010.