Analysis of mitochondrial DNA variations in a Chinese family with spinocerebellar ataxia-Reference-Cited by-同舟云学术

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Analysis of mitochondrial DNA variations in a Chinese family with spinocerebellar ataxia

Published:2012-01 Issue:1 Volume:19 Page:60-64
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Zeng Aiping,Liu Xinwei,Shen Lijun,Li Weizhen,Ding Zhongying,Bai Yidong,Lu Jianxin

Publisher

Elsevier BV

Subject

Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery

Reference28 articles.

1. The spinocerebellar ataxias;Gilman;Clin Neuropharmacol,2000

2. Glutamine repeats and neurodegeneration;Zoghbi;Annu Rev Neurosci,2000

3. Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology;Stevanin;Eur J Hum Genet,2000

4. DNA damage induced by polyglutamine-expanded proteins;Giuliano;Hum Mol Genet,2003

5. Early mitochondrial calcium defects in Huntington’s disease are a direct effect of polyglutamines;Panov;Nat Neurosci,2002

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1. Mechanisms;Migraine in Medicine;2022

2. Profiling of mitochondrial genomes in SCA3/MJD patients from mainland China;Gene;2020-05

3. New CACNA1A deletions are associated to migraine phenotypes;The Journal of Headache and Pain;2018-08-30

4. Accumulation of Mitochondrial DNA Common Deletion Since The Preataxic Stage of Machado-Joseph Disease;Molecular Neurobiology;2018-04-21

5. Towards the Identification of Molecular Biomarkers of Spinocerebellar Ataxia Type 3 (SCA3)/Machado-Joseph Disease (MJD);Polyglutamine Disorders;2018

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