New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease-Reference-Cited by-同舟云学术

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New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease

Published:1995-10-01 Issue:10 Volume:45 Page:1863-1866
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Bone L.J.,Dahl N.,Lensch M.W.,Chance P. F.,Kelly T.,Guern E. L.,Magi S.,Parry G.,Shapiro H.,Wang S.,Fischbeck K. H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 71 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. Clinical and electrophysiological characteristics of women with X‐linked Charcot–Marie–Tooth disease;European Journal of Neurology;2023-07-05

2. Generation of induced pluripotent stem cell (iPSC) line from a 36-year-old Charcot-Marie-Tooth disease patient with GJB1 mutation (CMTX);Stem Cell Research;2017-05

3. Phenotypes and cellular effects ofGJB1mutations causing CMT1X in a cohort of 226 Chinese CMT families;Clinical Genetics;2017-03-08

4. X-linked neuropathy of the Charcot-Marie-Tooth type;Peripheral nerve disorders;2014-08-11

5. Recurrent central nervous system white matter changes in charcot-Marie-Tooth type X disease;Muscle & Nerve;2014-01-27

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