Peripheral neuropathies caused by mutations in the myelin protein zero
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference64 articles.
1. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1;Bird;Am J Hum Genet,1982
2. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene;Hayasaka;Nat Genet,1993
3. Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A;Krajewski;Brain,2000
4. Electrophysiological features of inherited demyelinating neuropathies: a reappraisal in the era of molecular diagnosis;Lewis;Muscle Nerve,2000
5. 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
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2. Bone marrow stromal cell-conditioned medium regenerates injured sciatic nerve by increasing expression of MPZ and NGF and decreasing apoptosis;IRAN J BASIC MED SCI;2024
3. The cytoplasmic tail of myelin protein zero induces morphological changes in lipid membranes;2024-03-22
4. Structural bases for the Charcot-Marie-Tooth disease induced by single amino acid substitutions of myelin protein zero;Structure;2023-11
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