TGM6 gene mutations in undiagnosed cerebellar ataxia patients-Reference-Cited by-同舟云学术

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TGM6 gene mutations in undiagnosed cerebellar ataxia patients

Published:2018-01 Issue: Volume:46 Page:84-86
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Yang Zhi-hua,Shi Meng-meng,Liu Yu-tao,Wang Yan-lin,Luo Hai-yang,Wang Zhi-lei,Shi Chang-he,Xu Yu-ming

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference5 articles.

1. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing;Wang;Brain a J. Neurology,2010

2. Whole exome sequencing identifies a novel mutation in the transglutaminase 6 gene for spinocerebellar ataxia in a Chinese family;Li;Clin. Genet.,2013

3. Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization;Guo;Neurology,2014

4. Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia;Fogel;Mov. Disord. official J. Mov. Disord. Soc.,2012

5. Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase Z;Grenard;J. Biol. Chem.,2001

Cited by 9 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. Intragenic L1 Insertion: One Possibility of Brain Disorder;Life;2022-09-13

2. Clinical Spectrum of TGM6-Related Movement Disorders: A New Report with a Pooled Analysis of 48 Patients;Journal of Neurosciences in Rural Practice;2021-09-20

3. Neither a Novel Tau Proteinopathy nor an Expansion of a Phenotype: Reappraising Clinicopathology-Based Nosology;International Journal of Molecular Sciences;2021-07-07

4. TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study;Gene;2021-05

5. A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation;BMC Neurology;2020-11-07

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