Recurrent central nervous system white matter changes in charcot-Marie-Tooth type X disease
Author:
Affiliation:
1. Division of Child Neurology; Nationwide Children's Hospital; 700 Children's Drive Columbus Ohio 43205 USA
2. Department of Pediatrics; Ohio State University; Columbus Ohio USA
3. Department of Neurology; Ohio State University; Columbus Ohio USA
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24108/fullpdf
Reference13 articles.
1. CMT1X phenotypes represent loss of GJB1 gene function;Shy;Neurology,2007
2. New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease;Bone;Neurology,1995
3. X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode;Anand;Dev Med Child Neurol,2010
4. X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter;Basri;Intern Med,2007
5. Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation;Hanemann;Arch Neurol,2003
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