Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia-Reference-Cited by-同舟云学术

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Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

Published:2006-03-13 Issue:5 Volume:66 Page:654-659
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Elleuch N.,Depienne C.,Benomar A.,Hernandez A. M. O.,Ferrer X.,Fontaine B.,Grid D.,Tallaksen C.M.E.,Zemmouri R.,Stevanin G.,Durr A.,Brice A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 93 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. Spastic Paraplegia Type 7-Associated Optic Neuropathy: A Case Series;Journal of Neuro-Ophthalmology;2023-11-20

2. Spastic Paraplegia Type 7 (SPG7);Essentials of Cerebellum and Cerebellar Disorders;2023

3. Autosomal and X-Linked Degenerative Ataxias: From Genetics to Promising Therapeutics;Contemporary Clinical Neuroscience;2023

4. Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia;American Journal of Medical Genetics Part A;2022-11-11

5. A novel homozygous variant in the SPG7 gene presenting with childhood optic nerve atrophy;American Journal of Ophthalmology Case Reports;2022-06

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