Clinical features of hereditary spastic paraplegia due to spastin mutation-Reference-Cited by-同舟云学术

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Clinical features of hereditary spastic paraplegia due to spastin mutation

Published:2006-07-10 Issue:1 Volume:67 Page:45-51
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

McDermott C. J.,Burness C. E.,Kirby J.,Cox L. E.,Rao D. G.,Hewamadduma C.,Sharrack B.,Hadjivassiliou M.,Chinnery P. F.,Dalton A.,Shaw P. J.,

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 109 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. Hereditäre spastische Spinalparalysen erkennen und behandeln;NeuroTransmitter;2024-08

2. A novel truncated variant in SPAST results in spastin accumulation and defects in microtubule dynamics;BMC Medical Genomics;2023-12-08

3. Cohort analysis of novel SPAST variants in SPG4 patients and implementation of in vitro and in vivo studies to identify the pathogenic mechanism caused by splicing mutations;Frontiers in Neurology;2023-12-07

4. Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanisms;Expert Review of Proteomics;2023-09-02

5. Clinical features and genetic spectrum of Chinese patients with hereditary spastic paraplegia: A 14-year study;Frontiers in Genetics;2023-02-27

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