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History
- Received February 17, 2020
- Revision received June 1, 2020
- Accepted June 3, 2020
- Published online June 11, 2020.
Copyright & Usage
© 2020 Müller et al. This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
Author Information
- Juliane S Müller1,2,*,
- David T Burns1,3,*,
- Helen Griffin1,*,
- Graeme R Wells3,
- Romance A Zendah3,
- Benjamin Munro1,2,
- Claudia Schneider3,* and
- Rita Horvath1,2,*⇑
- 1Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK
- 2Department of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge, UK
- 3Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK
- Correspondence: Rh732{at}medschl.cam.ac.uk
↵* Juliane S Müller, David T Burns, Helen Griffin, Claudia Schneider, and Rita Horvath contributed equally to this work
Funding
Medical Research Council (UK)
MR/N025431/1R HorvathWellcome Investigator Award
109915/Z/15/ZR HorvathThe Newton Fund
MR/N027302/1R HorvathThe Wellcome Centre for Mitochondrial Research
203105/Z/16/ZR HorvathRoyal Society (UK)
UF150691C SchneiderBiotechnology and Biological Sciences Research Council/Medical Research Council (UK)
BB/R00143X/1C Schneider
Exosome in pontocerebellar hypoplasia
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