Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathy
Author:
Affiliation:
1. Neuropathology, IRCCS Foundation; “Carlo Besta” Neurological Institute; Milan; Italy
Publisher
Wiley
Subject
Neurology (clinical),General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1529-8027.2012.00443.x/fullpdf
Reference11 articles.
1. Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful neuropathy;Burns;Neuromuscul Disord,2006
2. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype;De Jonghe;Brain,1999
3. Immunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a);Gabriel;J Neurol Neurosurg Psychiatry,2002
4. The phenotype of Charcot-Marie-Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy;Houlden;Neuromuscul Disord,2009
5. Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis;Kilfoyle;J Neurol Neurosurg Psychiatry,2006
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1. Charcot–Marie–Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber Neuropathy;International Journal of Molecular Sciences;2024-01-29
2. Disease Progression in Charcot–Marie–Tooth Disease Related to MPZ Mutations: A Longitudinal Study;Annals of Neurology;2022-10-28
3. Mechanisms and Treatments in Demyelinating CMT;Neurotherapeutics;2021-10
4. New evidence for secondary axonal degeneration in demyelinating neuropathies;Neuroscience Letters;2021-01
5. 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
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