α-Synuclein gene duplication is present in sporadic Parkinson disease
Citation Manager Formats
Make Comment
See Comments

This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased.
To the Editor:
We read the article by Ahn et al. with great interest.1
As part of a similar study, we recently tested 403 patients with a diagnosis of Parkinson disease (PD) (234 men, mean age at onset: 48.0 ± 11.6 years) for gene dosage changes of SNCA by quantitative duplex PCR (n = 292) or MLPA (n = 111).2 We detected one SNCA duplication in a 38-year-old woman with a 2-year history of parkinsonism (1/403; 0.25%; figure e-1 on the Neurology® Web site at www.neurology.org), which is comparable to the number reported by Ahn et al. in a Korean PD population (3/906 = 0.3%).
Neurologic examination of our patient revealed generalized bradykinesia, rigidity predominantly of her right limbs, and mild postural instability but no rest tremor (UPDRS-III score: 32/108). We also …
AAN Members
We have changed the login procedure to improve access between AAN.com and the Neurology journals. If you are experiencing issues, please log out of AAN.com and clear history and cookies. (For instructions by browser, please click the instruction pages below). After clearing, choose preferred Journal and select login for AAN Members. You will be redirected to a login page where you can log in with your AAN ID number and password. When you are returned to the Journal, your name should appear at the top right of the page.
AAN Non-Member Subscribers
Purchase access
For assistance, please contact:
AAN Members (800) 879-1960 or (612) 928-6000 (International)
Non-AAN Member subscribers (800) 638-3030 or (301) 223-2300 option 3, select 1 (international)
Sign Up
Information on how to subscribe to Neurology and Neurology: Clinical Practice can be found here
Purchase
Individual access to articles is available through the Add to Cart option on the article page. Access for 1 day (from the computer you are currently using) is US$ 39.00. Pay-per-view content is for the use of the payee only, and content may not be further distributed by print or electronic means. The payee may view, download, and/or print the article for his/her personal, scholarly, research, and educational use. Distributing copies (electronic or otherwise) of the article is not allowed.
Letters: Rapid online correspondence
REQUIREMENTS
You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
Dr. David E. Vaillancourt and Dr. Shannon Y. Chiu
► Watch
Alert Me
Recommended articles
-
Articles
Early-onset parkinsonism associated with PINK1 mutationsFrequency, genotypes, and phenotypesV. Bonifati, C. F. Rohé, G. J. Breedveld et al.Neurology, July 11, 2005 -
Articles
Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal gangliaF. Binkofski, K. Reetz, C. Gaser et al.Neurology, August 27, 2007 -
Articles
Progression of subtle motor signs in PINK1 mutation carriers with mild dopaminergic deficitC. Eggers, A. Schmidt, J. Hagenah et al.Neurology, May 31, 2010 -
Articles
Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonismE. Moro, J. Volkmann, I. R. König et al.Neurology, March 31, 2008