CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
Saskia B. Wortmann(Radboud University Medical Center), Ron A. Wevers(Radboud University Nijmegen), Ania C. Muntau(University Medical Center Hamburg-Eppendorf), Michèl A.A.P. Willemsen(Radboud University Nijmegen), Christelle Golzio(Centre National de la Recherche Scientifique), Felix Distelmaier(Düsseldorf University Hospital), Søren W. Gersting(Ludwig-Maximilians-Universität München), Frédéric M. Vaz(Netherlands Metabolomics Centre), Joy Yaplito‐Lee(Royal Children's Hospital), Hans van Bokhoven(Radboud University Nijmegen), Joop H. Jansen(Radboud University Nijmegen), Katrin Õunap(Tartu University Hospital), Christine Klein(University of Lübeck), Maria Kousi, Arjan P.M. de Brouwer(Radboud University Nijmegen), Ewa Pronicka(Children's Memorial Health Institute), Rafał Płoski(Medical University of Warsaw), Elżbieta Chruściel(University of Gdańsk), Nicholas Katsanis(Io Therapeutics (United States)), G. Herma Renkema(Radboud University Nijmegen), Johannes N. Spelbrink(Radboud University Nijmegen), Szymon Ziętkiewicz(University of Gdańsk), Holger Prokisch(Helmholtz Zentrum München), Mia L. Pras‐Raves(Amsterdam UMC Location University of Amsterdam), Radek Szklarczyk(Maastricht University Medical Centre), Richard J. Rodenburg(Radboud University Nijmegen), Tim M. Strom(Technical University of Munich), Yolanda Lillquist(BC Children's Hospital), Riina Žordania(Tartu University Hospital), M. Estela Rubio‐Gozalbo(Maastricht University), Clara D.M. van Karnebeek(Amsterdam University Medical Centers), Tobias B. Haack(Technical University of Munich), Aleksandar Raković(University of Lübeck), Thomas Lücke(St. Josef-Hospital), Thomas Meitinger(Helmholtz Zentrum München)
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