A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function-Reference-Cited by-同舟云学术

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A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function

Published:2014-08-06 Issue:10 Volume:83 Page:903-912
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Tsai P.-C.,Huang Y.-H.,Guo Y.-C.,Wu H.-T.,Lin K.-P.,Tsai Y.-S.,Liao Y.-C.,Liu Y.-T.,Liu T.-T.,Kao L.-S.,Yet S.-F.,Fann M.-J.,Soong B.-W.,Lee Y.-C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 43 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. Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia;Annals of Clinical and Translational Neurology;2024-06-04

2. A pan-SARS-CoV-2-specific soluble angiotensin-converting enzyme 2-albumin fusion engineered for enhanced plasma half-life and needle-free mucosal delivery;PNAS Nexus;2023-11-28

3. Fibril structures of TFG protein mutants validate the identification of TFG as a disease-related amyloid protein by the IMPAcT method;PNAS Nexus;2023-11-20

4. NovelTFGmutation causes autosomal-dominant spastic paraplegia and defects in autophagy;Journal of Medical Genetics;2023-10-27

5. Decoding hereditary spastic paraplegia pathogenicity through transcriptomic profiling;Zoological Research;2023

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