PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson’s disease-Reference-Cited by-同舟云学术

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PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson’s disease

Published:2008-01-11 Issue:5 Volume:115 Page:715-719
ISSN:0300-9564
Container-title:Journal of Neural Transmission
language:en
Short-container-title:J Neural Transm

Author:

Chan Daniel Kam Yin,Mok Vincent,Ng Ping Wing,Yeung Jonas,Kwok John B.,Fang Zhi Ming,Clarke Raymond,Wong Lawrence,Schofield Peter R.,Hattori Nobutaka

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Psychiatry and Mental health,Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00702-007-0011-6.pdf

Reference9 articles.

1. Chan DKY, Cordato D, Bui Triet, Mellick G (2004) Comparison of environmental and genetic factors for Parkinson’s disease between Chinese and Caucasians. Neuroepidemiology 23:13–22

2. Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y (1998) Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals. Ann Neurol 44:935–941

3. Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N (1998) Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392:605–608

4. Lücking C, Durr A, Bonifati V, Jenny Vaughan J, De Michele G, Gasser T, Harhangi BS, Meco G, Denèfle P, Wood NW, Agid Y, Brice A (2000) Association between early-onset Parkinson’s disease and mutations in the Parkin gene. N Engl J Med 342:1560–1567

5. Mata I, Lockhart P, Farrer M (2004) Parkin genetics: one model for Parkinson’s disease. Hum Mol Genet 16:R127–R133

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1. A novel variant of PLA2G6 gene related early-onset parkinsonism: a case report and literature review;Frontiers in Neurology;2024-04-18

2. Case Report: A case of PLA2G6 gene-related early-onset Parkinson's disease and review of literature;Frontiers in Neuroscience;2022-12-09

3. A Han Chinese Family With Early-Onset Parkinson's Disease Carrying Novel Frameshift Mutation and Compound Heterozygous Mutation of PRKN Appearing Incompatible With MDS Clinical Diagnostic Criteria;Frontiers in Neurology;2020-10-09

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

5. Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes;Parkinsonism & Related Disorders;2019-12

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