SCA31 is rare in the Chinese population on Taiwan-Reference-Cited by-同舟云学术

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SCA31 is rare in the Chinese population on Taiwan

Published:2012-02 Issue:2 Volume:33 Page:426.e23-426.e24
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Lee Yi-Chung,Liu Chin-San,Lee Tzu-Ying,Lo Yang-Chung,Lu Yi-Chun,Soong Bing-Wen

Funder

National Science Council

Taipei Veterans General Hospital

Yen Tjing Ling Medical Foundation

Taiwan SCA association research fund

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

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1. Genetic Movement Disorders Commonly Seen in Asians;Movement Disorders Clinical Practice;2023-05-08

2. Spinocerebellar ataxia type 31 (SCA31);Journal of Human Genetics;2022-11-01

3. Mechanistic and Therapeutic Insights into Ataxic Disorders with Pentanucleotide Expansions;Cells;2022-05-06

4. Molecular Mechanisms in Pentanucleotide Repeat Diseases;Cells;2022-01-08

5. Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From Drosophila Model;Frontiers in Neuroscience;2021-05-25

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