Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia
Matias Wagner(Helmholtz Zentrum München), Rebecca Schüle(Institute of Human Genetics), Christoph Kernstock(STZ eyetrial), Maryam M. Hockley(University of Arizona), Selina Reich(German Center for Neurodegenerative Diseases), Abbas Tafakhori(Tehran University of Medical Sciences), Wolfgang Müller‐Felber(Ludwig-Maximilians-Universität München), Stephan Züchner(University of Miami), Maike Nagel(University of Tübingen), Daniel P. S. Osborn(University College London), Juliane Winkelmann(Helmholtz Zentrum München), Benedikt V. Hölbling(German Center for Neurodegenerative Diseases), Michael C. Kruer(Barrow Neurological Institute), Thomas Schwarzmayr(Helmholtz Zentrum München), Ulrike Ulmer(German Center for Neurodegenerative Diseases), Katharina Vill(Ludwig-Maximilians-Universität München), Neda Shahmohammadibeni(Semnan University of Medical Sciences), Yalda Jamshidi(St George's, University of London), Rim Amouri(Tunis University), Ehsan Ghayoor Karimiani(St George's, University of London), Reza Boostani(Mashhad University of Medical Sciences), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Sergio Padilla‐Lopez(Barrow Neurological Institute), Hossein Darvish(University of Social Welfare and Rehabilitation Sciences), Somayeh Bakhtiari(Barrow Neurological Institute), Ege Ozkan(St George's, University of London), Ina Gehweiler(German Center for Neurodegenerative Diseases), Fayçal Hentati(National Institute of Neurology Mongi-Ben Hamida), Jennifer Reichbauer(German Center for Neurodegenerative Diseases)
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