Analysis of Dosage Mutation inPARK2among Korean Patients with Early-Onset or Familial Parkinson's Disease-Reference-Cited by-同舟云学术

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Analysis of Dosage Mutation inPARK2among Korean Patients with Early-Onset or Familial Parkinson's Disease

Published:2014 Issue:3 Volume:10 Page:244
ISSN:1738-6586
Container-title:Journal of Clinical Neurology
language:en
Short-container-title:J Clin Neurol

Author:

Chu Min Kyung¹,Kim Won Chan²,Choi Jung Mi³,Hong Jeong-Hoon³,Kang Suk Yun¹,Ma Hyeo-Il¹,Kim Yun Joong¹³⁴

Affiliation:

1. Department of Neurology, Hallym University College of Medicine, Anyang, Korea.

2. Department of Neurology, CHA University College of Medicine, Pocheon, Korea.

3. Ilsong Institute of Life Science, Hallym University, Anyang, Korea.

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

Funder

Hallym University Medical Center

National Research Foundation of Korea

Publisher

Korean Neurological Association

Subject

Clinical Neurology,Neurology

Link

https://synapse.koreamed.org/pdf/10.3988/jcn.2014.10.3.244

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

2. Case report: Early-onset Parkinson's disease with initial spastic paraparesis and hyperreflexia caused by compound heterozygous PRKN-gene exon 2 and 4 deletions;Frontiers in Neurology;2022-11-17

3. A very early onset of juvenile parkinsonism;Journal of Neurology;2022-07-18

4. Novel ATP13A2 and PINK1 variants identified in Chinese patients with Parkinson’s disease by whole-exome sequencing;Neuroscience Letters;2020-08

5. The M458L missense mutation disrupts the catalytic properties of Parkin;FEBS Letters;2017-12-27

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