PLP1 mutations and central demyelination: Evidence from electrophysiologic phenotyping in female manifesting carriers

Neurol Clin Pract. 2017 Oct;7(5):451-454. doi: 10.1212/CPJ.0000000000000346.

Authors

Michael J Keogh¹, Stephan R Jaiser¹, Hannah E Steele¹, Rita Horvath¹, Patrick F Chinnery¹, Mark R Baker¹

Affiliation

¹ 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.

No abstract available

Publication types

Case Reports

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