Reply to: “Low Frequency of p. <scp>S510G</scp> in <scp>PIAS1</scp> Challenges Its Relevance for Modifying Repeat Expansion Disorders”-Reference-Cited by-同舟云学术

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Reply to: “Low Frequency of p. S510G in PIAS1 Challenges Its Relevance for Modifying Repeat Expansion Disorders”

Published:2022-10 Issue:10 Volume:37 Page:2169-2169
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Lee Yan Hua¹,Lee Yi‐Chung²,Tsai Yu‐Shuen³,Yang Ueng‐Cheng³⁴,Cheng Tzu‐Hao⁵,Chern Yijuang¹^ORCID,Soong Bing‐Wen⁶

Affiliation:

1. Institute of Biomedical Sciences Academia Sinica Taipei Taiwan

2. Department of Neurology, Taipei Veterans General Hospital, and Brain Research Center National Yang Ming Chiao Tung University Taipei Taiwan

3. Center for Systems and Synthetic Biology National Yang Ming Chiao Tung University Taipei Taiwan

4. Institute of Biomedical Informatics National Yang Ming Chiao Tung University Taipei Taiwan

5. Institute of Biochemistry and Molecular Biology, and Brain Research Center National Yang Ming Chiao Tung University Taipei Taiwan

6. Department of Neurology, Shuang Ho Hospital, and Taipei Neuroscience Institute Taipei Medical University Taipei Taiwan

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29192

Reference6 articles.

1. Low Frequency of p. S510G in PIAS1 Challenges its Relevance for Modifying Repeat Expansion Disorders

2. A PIAS1 Protective Variant S510G Delays polyQ Disease Onset by Modifying Protein Homeostasis

3. Huntington's disease: from molecular pathogenesis to clinical treatment

4. Frequency Analysis of Autosomal Dominant Cerebellar Ataxias in Taiwanese Patients and Clinical and Molecular Characterization of Spinocerebellar Ataxia Type 6

5. Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities

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