Phenotypic variation of a new P0 mutation in genetically identical twins-Reference-Cited by-同舟云学术

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Phenotypic variation of a new P0 mutation in genetically identical twins

Published:1999-07-22 Issue:7 Volume:246 Page:596-599
ISSN:0340-5354
Container-title:Journal of Neurology
language:
Short-container-title:Journal of Neurology

Author:

Marques Jr. Wilson,Hanna Michael G.,Marques Solana R.,Sweeney Mary G.,Thomas P. K.,Wood N. W.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s004150050410.pdf

Cited by 32 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 with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber Neuropathy;International Journal of Molecular Sciences;2024-01-29

2. Novel mutation in the MPZ gene causes early-onset but slow-progressive Charcot–Marie–Tooth disease in a Russian family: a case report;Journal of International Medical Research;2022-12

3. The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study;Clinical Neurophysiology;2018-01

4. Coexistent Charcot-Marie-Tooth type 1A and type 2 diabetes mellitus neuropathies in a Chinese family;Neural Regeneration Research;2015

5. Charcot-Marie-Tooth Disease, Psychiatric Indicators and Quality of Life: A Systematic Review;ASN Neuro;2014-03-27

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