Mutations in SACS cause atypical and late-onset forms of ARSACS-Reference-Cited by-同舟云学术

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Mutations in SACS cause atypical and late-onset forms of ARSACS

Published:2010-09-27 Issue:13 Volume:75 Page:1181-1188
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Baets J.,Deconinck T.,Smets K.,Goossens D.,Van den Bergh P.,Dahan K.,Schmedding E.,Santens P.,Rasic V. M.,Van Damme P.,Robberecht W.,De Meirleir L.,Michielsens B.,Del-Favero J.,Jordanova A.,De Jonghe P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 111 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. HDAC inhibitor SAHA resolved intermediate filament bundling and defective autophagy caused by the lack of sacsin in ARSACS.;2024-08-17

2. Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix–Saguenay;Molecular Genetics & Genomic Medicine;2024-07

3. Compound Heterozygous Mutations of SACS in a Korean Cohort Study of Charcot-Marie-Tooth Disease Concurrent Cerebellar Ataxia and Spasticity;International Journal of Molecular Sciences;2024-06-09

4. Autosomal recessive cerebellar ataxias: a diagnostic classification approach according to ocular features;Frontiers in Integrative Neuroscience;2024-02-07

5. Vestibular Hypofunction in ARSACS Syndrome;Neurology Clinical Practice;2024-02

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