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May 10, 2024Open Access

Molecular Myelin Dysfunction in the Most Common Inherited Peripheral Neuropathies – CMT1A and HNPP

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Authors

KMKathryn R. MossEmory UniversityDGDave GutierrezRMRuifa MiJohns Hopkins University

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Cite This Study

Moss et al. (2024) studied this question.

synapsesocial.com/papers/68e6ac5ab6db64358762e967https://doi.org/10.1101/2024.05.10.592618
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Peripheral Myelin Protein-22 and Its Prominence in Charcot-Marie-Tooth Disease2026 · 1 citations
  2. 2Hereditary neuropathies caused by mutations in the gene encoding peripheral myelin protein 222025
  3. 3Longitudinal analysis of lipid changes in the sciatic nerve caused by overexpression of PMP22 in murine models of CMT1A2026 · 1 citations
  4. 4Delayed Genetic Diagnosis of a Rare Presentation of Overlapping Peripheral Myelin Protein 22 (PMP22) Neuropathies2026
  5. 5PMP22 duplication dysregulates lipid homeostasis and plasma membrane organization in developing human Schwann cells2024 · 28 citations