Novel SPG11 mutations in Chinese families with hereditary spastic paraplegia with thin corpus callosum-Reference-Cited by-同舟云学术

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Novel SPG11 mutations in Chinese families with hereditary spastic paraplegia with thin corpus callosum

Published:2013-03 Issue:3 Volume:19 Page:367-370
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Cao Li,Rong Tian-Yi,Huang Xiao-Jun,Fang Rong,Wu Zhi-Yuan,Tang Hui-Dong,Chen Sheng-Di

Funder

National Program of Basic Research

National Natural Science Fund

Key Discipline Program of Shanghai Municipality

Shanghai Key Project of Basic Science Research

Program for Outstanding Medical Academic Leader

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference12 articles.

1. Classification of the hereditary ataxias and paraplegias;Harding;Lancet,1983

2. Hereditary spastic paraplegias: an update;Depienne;Curr Opin Neurol,2007

3. Familial spastic paraplegia with mental impairment and thin corpus callosum;Nakamura;J Neurol Sci,1995

4. Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration;Stevanin;Brain,2008

5. Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum;Chen;Neurosci Lett,2008

Cited by 12 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. Case report: Novel mutations in the SPG11 gene in a case of autosomal recessive hereditary spastic paraplegia with a thin corpus callosum;Frontiers in Integrative Neuroscience;2023-03-24

2. Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers;Expert Review of Molecular Diagnostics;2022-07-03

3. Pluripotent Stem Cell Derived Neurons as In Vitro Models for Studying Autosomal Recessive Parkinson’s Disease (ARPD): PLA2G6 and Other Gene Loci;Advances in Experimental Medicine and Biology;2021

4. Genetic mutation analysis of hereditary spastic paraplegia;Medicine;2020-06-05

5. Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11;BMC Neurology;2020-01-03

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