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

by Moggio Maurizio, Capovilla Giuseppe, Cagdas Sophie, Collotta Martina, Sciacco Monica, Rizzuti Mafalda, Fortunato Francesco, Bordoni Andreina, Orcesi Simona, Tonduti Davide, Cosi Alessandra, Ronchi Dario, Berardinelli Angela, Veggiotti Pierangelo, Comi Giacomo P
Published 2011-07-01