Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias-Reference-Cited by-同舟云学术

Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias

Published:2021-08 Issue: Volume:89 Page:120-127
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Wan Na,Chen Zhao,Wan Linlin,Yuan Hongyu,Tang Zhichao,Liu Mingjie,Peng Yun,Peng Linliu,Lei Lijing,Xie Yue,Deng Qi,Wang Shang,Wang Chunrong,Peng Huirong,Hou Xuan,Shi Yuting,Long Zhe,Qiu Rong,Xia Kun,Tang Beisha,Jiang Hong

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference30 articles.

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2. Co-occurrence of ATXN3 and ATXN2 repeat expansions in Chinese ataxia patients with slow saccades;Wu;Mol Genet Genomic Med,2019

3. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6;Izumi;Am. J. Hum. Genet.,2003

4. SCA8 repeat expansion coexists with SCA1--not only with SCA6;Sulek;Am. J. Hum. Genet.,2003

5. Two in one: report of a patient with spinocerebellar ataxia types 2 and 10;Kapur;Arch. Neurol.,2012

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3. Diagnostic Yield of NGS Tests for Hereditary Ataxia: a Systematic Review;The Cerebellum;2023-11-11

4. Early-onset familial essential tremor is associated with nucleotide expansions of spinocerebellar ataxia in China;2023-05-15

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