Myelin protein zero: Mutations in the cytoplasmic domain interfere with its cellular trafficking
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Reference35 articles.
1. Identification of a 4 bp deletion (1560de14) in Po gene in a family with severe charcot-Marie-Tooth disease
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3. A Phorbol Ester-Sensitive Kinase Catalyzes the Phosphorylation of P0Glycoprotein in Myelin
4. Mutational analysis ofPMP22, MPZ, GJB1, EGR2 andNEFL in Korean Charcot-Marie-Tooth neuropathy patients
5. The cytoplasmic domain of myelin glycoprotein P0 interacts with negatively charged phospholipid bilayers.
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2. Defective axonal transport: A common pathological mechanism in inherited and acquired peripheral neuropathies;Neurobiology of Disease;2017-09
3. Polarization and Myelination in Myelinating Glia;ISRN Neurology;2012-12-30
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5. Molecular basis of axonal dysfunction and traffic impairments in CMT;Brain Research Bulletin;2012-08
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