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PDFNeurological rarities
Diagnosis of spinal xanthomatosis by next-generation sequencing: identifying a rare, treatable mimic of hereditary spastic paraparesis
- Correspondence to Professor Pamela J Shaw, Sheffield Institute for Translational Neuroscience, University of Sheffield, 385A Glossop Road, Sheffield S10 2HQ, UK; pamela.shaw{at}sheffield.ac.uk
Citation
Diagnosis of spinal xanthomatosis by next-generation sequencing: identifying a rare, treatable mimic of hereditary spastic paraparesis
Publication history
- Accepted March 10, 2015
- First published April 10, 2015.
Online issue publication
July 14, 2015
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- Previous version (10 April 2015).
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