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1 Department of Psychiatry, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA.
2 Department of Psychiatry, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA; Medical Scientist Training Program, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA.
3 Department of Neurology, School of Medicine, Washington University in St Louis, Saint Louis, MO, USA.
4 Department of Medicine, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA.
5 Department of Psychiatry, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA; Hope Center Program on Protein Aggregation and Neurodegeneration, Washington University in Saint Louis, Saint Louis, MO, USA. Electronic address: ccruchaga@wustl.edu.
1 Department of Psychiatry, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA.
2 Department of Psychiatry, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA; Medical Scientist Training Program, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA.
3 Department of Neurology, School of Medicine, Washington University in St Louis, Saint Louis, MO, USA.
4 Department of Medicine, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA.
5 Department of Psychiatry, School of Medicine, Washington University in Saint Louis, Saint Louis, MO, USA; Hope Center Program on Protein Aggregation and Neurodegeneration, Washington University in Saint Louis, Saint Louis, MO, USA. Electronic address: ccruchaga@wustl.edu.
A study on familial Parkinson disease (PD) described 4 variants in the gene TMEM230 (Chr. 20p13) as the cause of PD. The aim of this study was to test if variants in the TMEM230 gene are associated with PD in 2 independent American European data sets. No variants in the TMEM230 region were found associated with PD, age at onset, or cerebrospinal fluid α-synuclein levels.
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, et al. Identification of TMEM230 mutations in familial Parkinson’s disease. Nat Genet. 2016;48(7):733–9.
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de Lau LM, Breteler MM. Epidemiology of Parkinson’s disease. The Lancet Neurology. 2006;5(6):525–35.
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Kalinderi K, Bostantjopoulou S, Fidani L. The genetic background of Parkinson’s disease: current progress and future prospects. Acta Neurol Scand. 2016;134(5):314–26.
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Giri A, Mok KY, Jansen I, Sharma M, Tesson C, Mangone G, et al. Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson’s disease in the Caucasian population. Neurobiology of aging. 2016
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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.
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