Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease-Reference-Cited by-同舟云学术

Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease

Published:2005-12-15 Issue:2 Volume:59 Page:298-309
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Nishioka Kenya¹,Hayashi Shin²,Farrer Matthew J.³,Singleton Andrew B.⁴,Yoshino Hiroyo⁵,Imai Hisamasa⁶,Kitami Toshiaki¹,Sato Kenichi¹,Kuroda Ryu⁷,Tomiyama Hiroyuki¹⁷,Mizoguchi Koichi⁷,Murata Miho⁸⁹,Toda Tatsushi⁹¹⁰,Imoto Issei²,Inazawa Johji²,Mizuno Yoshikuni¹⁵,Hattori Nobutaka¹⁵⁹

Affiliation:

1. Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan

2. Department of Molecular Cytogenetics, Medical Research Institute and Graduate School of Biomedical Science, Tokyo Medical and Dental University, Tokyo, Japan

3. Department of Neuroscience, Mayo Clinic, Jacksonville, FL

4. Laboratory of Neurogenetics, National Institute on Aging, Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, Genetic Diseases Research Branch, National Institute of Health, Bethesda, MD

5. Research Institute for Disease of Old Ages, Juntendo University School of Medicine

6. Deparment of Neurology, Tokyo Rinkai Hospital, Tokyo

7. Department of Neurology, Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka

8. Department of Neurology, Musashi Hospital, National Center of Neurology and Psychiatry, Kodaira

9. CREST, Japan Science and Technology Corporation, Kawaguchi, Saitama, Japan

10. Division of Functional Genomics, Osaka University Graduate School of Medicine, Suita, Japan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.20753

Reference36 articles.

1. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

2. A susceptibility locus for Parkinson's disease maps to chromosome 2p13

3. A susceptibility gene for late-onset idiopathic Parkinson's disease

4. The ubiquitin pathway in Parkinson's disease

5. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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