A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK-Reference-Cited by-同舟云学术

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

Published:2017-04-18 Issue:6 Volume:140 Page:1611-1618
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

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)

Link

http://academic.oup.com/brain/article-pdf/140/6/1611/24175071/awx082.pdf

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