Novel C59T leader peptide mutation in the MPZ gene associated with late-onset, axonal, sensorimotor polyneuropathy
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2006.01479.x/fullpdf
Reference17 articles.
1. Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation
2. Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembraneMPZ mutation
3. Phenotypic clustering in MPZ mutations
4. A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B
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2. New evidence for secondary axonal degeneration in demyelinating neuropathies;Neuroscience Letters;2021-01
3. Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype;Journal of Neurology;2019-07-05
4. Myelinating Glia-Specific Deletion of Fbxo7 in Mice Triggers Axonal Degeneration in the Central Nervous System Together with Peripheral Neuropathy;The Journal of Neuroscience;2019-05-13
5. A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia;Clinical Neurology and Neurosurgery;2010-11
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