Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
Monika Hartig(Technical University of Munich), Arcangela Iuso(Helmholtz Zentrum München), Tobias B. Haack(Helmholtz Zentrum München), Tomasz Kmieć(Children's Memorial Health Institute), Elżbieta Jurkiewicz(Children's Memorial Health Institute), Katharina Heim(Helmholtz Zentrum München), Sigrun Roeber(Ludwig-Maximilians-Universität München), Victoria Tarabin(University of Regensburg), Sabrina Dusi(Fondazione IRCCS Istituto Neurologico Carlo Besta), Małgorzata Krajewska‐Walasek(Children's Memorial Health Institute), Sergiusz Jóźwiak(Children's Memorial Health Institute), Maja Hempel(Helmholtz Zentrum München), Juliane Winkelmann(Helmholtz Zentrum München), Matthias Elstner(Helmholtz Zentrum München), Konrad Oexle(Technical University of Munich), Thomas Klopstock(Ludwig-Maximilians-Universität München), Wolfgang Mueller‐Felber(Ludwig-Maximilians-Universität München), Thomas Gasser(German Center for Neurodegenerative Diseases), Claudia Trenkwalder(Paracelsus Elena Klinik Kassel), Valeria Tiranti(Fondazione IRCCS Istituto Neurologico Carlo Besta), Hans A. Kretzschmar(Ludwig-Maximilians-Universität München), Gerd Schmitz(University of Regensburg), Tim M. Strom(Helmholtz Zentrum München), Thomas Meitinger(Helmholtz Zentrum München), Holger Prokisch(Helmholtz Zentrum München)
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