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Items: 4

1.
Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot–Marie–Tooth disease type 1C
Samuel M. Lee, Di Sha, Anum A. Mohammed, Seneshaw Asress, Jonathan D. Glass, Lih-Shen Chin, Lian Li
Hum Mol Genet. 2013 May 1; 22(9): 1755–1770. Published online 2013 Jan 28. doi: 10.1093/hmg/ddt022
PMCID:
PMC3613163
AbstractArticlePDF–1.2M
2.
Mutations associated with Charcot–Marie–Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome–autophagy pathways
Samuel M. Lee, James A. Olzmann, Lih-Shen Chin, Lian Li
J Cell Sci. 2011 Oct 1; 124(19): 3319–3331. doi: 10.1242/jcs.087114
PMCID:
PMC3178453
AbstractArticle
3.
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
P F Chance, T D Bird, P O'Connell, H Lipe, J M Lalouel, M Leppert
Am J Hum Genet. 1990 Dec; 47(6): 915–925.
PMCID:
PMC1683894
SummaryPage BrowsePDF–1.1M
4.
Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies
Valerie A. Street, Jeff D. Goldy, Alana S. Golden, Bruce L Tempel, Thomas D. Bird, Phillip F. Chance
Am J Hum Genet. 2002 Jan; 70(1): 244–250. Published online 2001 Nov 16. doi: 10.1086/337943
PMCID:
PMC384893
AbstractArticlePDF–140K

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