SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3-Reference-Cited by-同舟云学术

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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

Published:2013-06-07 Issue:2 Volume:81 Page:165-173
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Nakhro K.,Park J.-M.,Hong Y. B.,Park J. H.,Nam S. H.,Yoon B. R.,Yoo J. H.,Koo H.,Jung S.-C.,Kim H.-L.,Kim J. Y.,Choi K.-G.,Choi B.-O.,Chung K. W.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 59 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. Styxl2 regulates de novo sarcomere assembly by binding to non-muscle myosin IIs and promoting their degradation;eLife;2024-06-03

2. Identification of a Novel Homozygous Mutation in MTMR2 Gene Causes Very Rare Charcot–Marie–Tooth Disease Type 4B1;The Application of Clinical Genetics;2024-05

3. Characterization of a novel zebrafish model ofMTMR5-associated CMT4B3;2024-04-20

4. Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy;Journal of Neurogenetics;2024-04-02

5. Styxl2 regulates de novo sarcomere assembly by binding to non-muscle myosin IIs and promoting their degradation;ELIFE;2024-01-23

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