PLP1 mutations and central demyelination
Evidence from electrophysiologic phenotyping in female manifesting carriers
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Article Information
- Received November 21, 2016
- Accepted January 30, 2017
- First Published March 8, 2017.
Article Versions
- Previous version (March 8, 2017 - 13:00).
- You are viewing the most recent version of this article.
Author Disclosures
- Michael J. Keogh, MRCP,
- Stephan R. Jaiser, PhD, MRCP,
- Hannah E. Steele, MRCP,
- Rita Horvath, MD, PhD,
- Patrick F. Chinnery, PhD, FRCP, FMedSci and
- Mark R. Baker, PhD, MRCP
- Michael J. Keogh, MRCP,
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- Stephan R. Jaiser, PhD, MRCP,
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- Hannah E. Steele, MRCP,
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1) Salary support received from GSK.
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- Rita Horvath, MD, PhD,
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- Patrick F. Chinnery, PhD, FRCP, FMedSci and
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BRAIN, Associate Editor 2004
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Medical Research Council (UK) NIHR (England)
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Wellcome Trust
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- Mark R. Baker, PhD, MRCP
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NIHR (supported lab research - to present) MRC (supported lab research - to present)
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- Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Centre for Life (MJK, HES, RH, PFC), and Institute of Neuroscience (SRJ, MRB), Newcastle University; Departments of Neurology (MJK, SRJ, HES, RH, PFC, MRB) and Neurophysiology (SRJ, MRB), Royal Victoria Infirmary, Newcastle Upon Tyne; and Department of Clinical Neurosciences (MJK, PFC), University Neurology Unit, Cambridge Biomedical Campus, UK.
- Correspondence to:
mjk72{at}cam.ac.uk
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