CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
Titel:
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
Auteur:
Wortmann, Saskia B. Ziętkiewicz, Szymon Kousi, Maria Szklarczyk, Radek Haack, Tobias B. Gersting, Søren W. Muntau, Ania C. Rakovic, Aleksandar Renkema, G. Herma Rodenburg, Richard J. Strom, Tim M. Meitinger, Thomas Rubio-Gozalbo, M. Estela Chrusciel, Elzbieta Distelmaier, Felix Golzio, Christelle Jansen, Joop H. van Karnebeek, Clara Lillquist, Yolanda Lücke, Thomas Õunap, Katrin Zordania, Riina Yaplito-Lee, Joy van Bokhoven, Hans Spelbrink, Johannes N. Vaz, Frédéric M. Pras-Raves, Mia Ploski, Rafal Pronicka, Ewa Klein, Christine Willemsen, Michel A.A.P. de Brouwer, Arjan P.M. Prokisch, Holger Katsanis, Nicholas Wevers, Ron A.