Mutations inTUBB4Aand spastic paraplegia-Reference-Cited by-同舟云学术

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Mutations inTUBB4Aand spastic paraplegia

Published:2015-10-19 Issue:13 Volume:30 Page:1857-1858
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Kumar Kishore R.¹²,Vulinovic Franca³,Lohmann Katja³,Park Jin-Sung¹,Schaake Susen³,Sue Carolyn M.¹,Klein Christine³

Affiliation:

1. Department of Neurogenetics, Kolling Institute of Medical Research and Royal North Shore Hospital; The University of Sydney; Australia

2. Kinghorn Centre for Clinical Genomics; Garvan Institute of Medical Research; Darlinghurst Sydney Australia

3. Institute of Neurogenetics; University of Lübeck; Lübeck Germany

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference8 articles.

1. Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia;Kancheva;Mov Disord,2015

2. Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene;Lohmann;Ann Neurol,2013

3. A de novo mutation in the beta-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum;Simons;Am J Hum Genet,2013

4. TUBB4A de novo mutations cause isolated hypomyelination;Pizzino;Neurology,2014

5. Hereditary spastic paraplegia: advances in genetic research;Fink;Neurology,1996

Cited by 4 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. Hereditary spastic paraplegia: Genetic heterogeneity and common pathways;Experimental Neurology;2022-11

2. TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes;Human Molecular Genetics;2017-08-29

3. Congenital-onset spastic paraplegia in a patient with TUBB4A mutation and mild hypomyelination;Journal of the Neurological Sciences;2016-09

4. Reply: Mutations inTUBB4Aand spastic paraplegia;Movement Disorders;2015-10-19

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