A Novel Heterozygous ANO3 Mutation with Basal Ganglia Dysfunction in a Patient with Adult-Onset Isolated Segmental Dystonia

Author:

Yoo Han Soo1,Lee Hyunjoo2,Chung Seok Jong1,Lee Jin-Sung2,Hong Sang-Kyoon3,Lee Phil Hyu1,Kim Yun Joong345,Sohn Young Ho1,Shin Hae-Won6

Affiliation:

1. Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.

2. Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.

3. Hallym Institute of Translational Genomics and Bioinformatics, Hallym University Medical Center, Anyang, Korea.

4. Department of Neurology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Korea.

5. ILSONG Institute of Life Science, Hallym University, Anyang, Korea.

6. Department of Neurology, Chung-Ang University College of Medicine, Seoul, Korea.

Publisher

Korean Neurological Association

Subject

Neurology (clinical),Neurology

Cited by 8 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. The Clinical Spectrum of ANO3—Report of a New Family and Literature Review;Movement Disorders Clinical Practice;2024-01-29

2. The expanding clinical and genetic spectrum of ANO3 dystonia;Neuroscience Letters;2021-02

3. ANO3 Mutations in Chinese Dystonia: A Genetic Screening Study Using Next-Generation Sequencing;Frontiers in Neurology;2020-02-07

4. Dystonia;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

5. Dystonia genes and their biological pathways;Neurobiology of Disease;2019-09

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