Effect of an R69C Mutation in the Myelin Protein Zero Gene on Myelination and Ion Channel Subtypes-Reference-Cited by-同舟云学术

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Effect of an R69C Mutation in the Myelin Protein Zero Gene on Myelination and Ion Channel Subtypes

Published:2006-12-01 Issue:12 Volume:63 Page:1787
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Bai Yunhong,Ianokova Emilia,Pu Qin,Ghandour Khaled,Levinson Rock,Martin Jean-Jacques,Ceuterick-de Groote Chantal,Mazanec Radim,Seeman Pavel,Shy Michael E.,Li Jun

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 41 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Charcot-Marie-Tooth Disease;Reference Module in Neuroscience and Biobehavioral Psychology;2024

2. Myelin protein zero mutation‐related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort;Brain Pathology;2023-08-15

3. Mechanisms and treatment strategies of demyelinating and dysmyelinating Charcot-Marie-Tooth disease;Neural Regeneration Research;2023

4. Disease Progression in Charcot–Marie–Tooth Disease Related to MPZ Mutations: A Longitudinal Study;Annals of Neurology;2022-10-28

5. Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice;Molecular Neurobiology;2022-04-30

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