Human Nerve Pathology Caused by Different Mutational Mechanisms of thePMP22Gene
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1999.tb08595.x/fullpdf
Reference56 articles.
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2. Charcot-Marie-Tooth disease and related peripheral neuropathies;Jonghe;J. Periph. Nerv. Syst.,1997
3. Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13);Snipes;J. Cell Biol.,1992
4. Ultrastructural distribution of PMP22 in Charcot-Marie-Tooth disease type 1A;Haney;J. Neuropathol. Exp. Neurol.,1996
5. Ins and outs of peripheral myelin protein-22: Mapping transmembrane topology and intracellular sorting;D'Urso;J. Neurosci. Res.,1997
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