A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK

Author:

Morgan Sarah1,Shatunov Aleksey2,Sproviero William2,Jones Ashley R.2,Shoai Maryam1,Hughes Deborah1,Al Khleifat Ahmad2,Malaspina Andrea3,Morrison Karen E.4,Shaw Pamela J.5,Shaw Christopher E.2,Sidle Katie6,Orrell Richard W.6,Fratta Pietro7,Hardy John1,Pittman Alan1,Al-Chalabi Ammar2

Affiliation:

1. Department of Molecular Neuroscience, UCL, Institute of Neurology, Queen Square, London, WC1N 3BG, UK

2. Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, King’s College London, SE5 9RX, UK

3. Centre for Neuroscience and Trauma, Blizard Institute, Queen Mary University of London, North-East London and Essex Regional Motor Neuron Disease Care Centre, London, E1 2AT, UK

4. Faculty of Medicine, University of Southampton, MP801 University Hospital Southampton NHS Foundation Trust, SO16 6YD, UK

5. Sheffield Institute for Translational Neuroscience (SiTraN), University of Sheffield, 385a Glossop Road, Sheffield, S10 2HQ, UK

6. Department of Clinical Neuroscience, UCL Institute of Neurology, Rowland Hill Street, London, NW3 2PF, UK

7. Department of Neurodegenerative Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK

Funder

Wellcome Trust

Medical Research Council

Economic and Social Research Council

European Community’s Health Seventh Framework Programme

Horizon 2020 Programme

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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