SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years-Reference-Cited by-同舟云学术

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Published:2006-01-09 Issue:1 Volume:66 Page:112-114
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Namekawa M.,Ribai P.,Nelson I.,Forlani S.,Fellmann F.,Goizet C.,Depienne C.,Stevanin G.,Ruberg M.,Durr A.,Brice A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 100 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. Patients with complex and very-early-onset ATL1-related spastic paraplegia offer insights on genotype/phenotype correlations and support for autosomal recessive forms of SPG3A;Journal of Neurology;2024-07-13

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4. Genetic and clinical features of pediatric-onset hereditary spastic paraplegia: a single-center study in Japan;Frontiers in Neurology;2023-05-12

5. Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis;Neurological Sciences;2022-11-28

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