The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease-Reference-Cited by-同舟云学术

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The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease

Published:2015-09-24 Issue:1 Volume:10 Page:
ISSN:1750-1326
Container-title:Molecular Neurodegeneration
language:en
Short-container-title:Mol Neurodegeneration

Author:

Mata Ignacio F.,Jang Yongwoo,Kim Chun-Hyung,Hanna David S.,Dorschner Michael O.,Samii Ali,Agarwal Pinky,Roberts John W.,Klepitskaya Olga,Shprecher David R.,Chung Kathryn A.,Factor Stewart A.,Espay Alberto J.,Revilla Fredy J.,Higgins Donald S.,Litvan Irene,Leverenz James B.,Yearout Dora,Inca-Martinez Miguel,Martinez Erica,Thompson Tiffany R.,Cholerton Brenna A.,Hu Shu-Ching,Edwards Karen L.,Kim Kwang-Soo,Zabetian Cyrus P.

Funder

National Institute of Neurological Disorders and Stroke

U.S. Department of Veterans Affairs

Dolsen Foundation

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13024-015-0045-4.pdf

Reference23 articles.

1. Trinh J, Farrer M. Advances in the genetics of Parkinson disease. Nat Rev Neurol. 2013;9(8):445–54.

2. Singleton AB. Exome sequencing: a transformative technology. Lancet Neurol. 2011;10(10):942–6.

3. Zimprich A, Benet-Pages A, Struhal W, Graf E, Eck SH, Offman MN, et al. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am J Hum Genet. 2011;89(1):168–75.

4. Vilarino-Guell C, Rajput A, Milnerwood AJ, Shah B, Szu-Tu C, Trinh J, et al. DNAJC13 mutations in Parkinson disease. Hum Mol Genet. 2014;23(7):1794–801.

5. Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson’s disease. J Neurol Neurosurg Psychiatry. 1988;51(6):745–52.

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