Charcot-Marie-Tooth disease
Author:
Publisher
Wiley
Subject
Neurology (clinical),General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1529-8027.2011.00324.x/fullpdf
Reference61 articles.
1. Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotype.;Abe;J Hum Genet,2009
2. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.;Antonellis;Am J Hum Genet,2003
3. Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review.;Auer-Grumbach;Arch Neurol,2003
4. Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation.;Auer-Grumbach;Ann Neurol,2005
5. SPTLC1 is mutated in hereditary sensory neuropathy, type 1.;Bejaoui;Nat Genet,2001
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