Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency
Titel:
Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency
Auteur:
Melchionda, Laura Haack, Tobias B. Hardy, Steven Abbink, Truus E.M. Fernandez-Vizarra, Erika Lamantea, Eleonora Marchet, Silvia Morandi, Lucia Moggio, Maurizio Carrozzo, Rosalba Torraco, Alessandra Diodato, Daria Strom, Tim M. Meitinger, Thomas Tekturk, Pinar Yapici, Zuhal Al-Murshedi, Fathiya Stevens, René Rodenburg, Richard J. Lamperti, Costanza Ardissone, Anna Moroni, Isabella Uziel, Graziella Prokisch, Holger Taylor, Robert W. Bertini, Enrico van der Knaap, Marjo S. Ghezzi, Daniele Zeviani, Massimo