Dilemma in differentiation of spinocerebellar ataxia type 17 from Huntington’s disease: comorbidity or independent disease?-Reference-Cited by-同舟云学术

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Dilemma in differentiation of spinocerebellar ataxia type 17 from Huntington’s disease: comorbidity or independent disease?

Published:2023-10-19 Issue: Volume: Page:1-5
ISSN:0020-7454
Container-title:International Journal of Neuroscience
language:en
Short-container-title:International Journal of Neuroscience

Author:

An Li¹,Yao Sheng¹,Liu Jianguo¹,Qi Xiaokun¹,Duan Feng¹,Sun Chenjing¹^ORCID

Affiliation:

1. Department of Neurology, The Sixth Medical Center of PLA General Hospital, Beijing, China

Publisher

Informa UK Limited

Subject

General Medicine,General Neuroscience

Link

https://www.tandfonline.com/doi/pdf/10.1080/00207454.2023.2273766

Reference15 articles.

1. The emerging roles of long non‐coding RNAs in polyglutamine diseases

2. Pay attention to repeat expansion mutation related neurogenetic diseases;Tang B;Chin J Neurol,2020

3. Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17

4. A series of cases with Huntington-like phenotype and intermediate repeats in HTT

5. Spinocerebellar Ataxia Type 17 (SCA17)

Cited by 1 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. Genetics of Huntington’s disease and related disorders: beyond triplet repeats;Ageing and Neurodegenerative Diseases;2024-02-29

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