A simple and efficient method for apolipoprotein E genotype determination
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.
There is currently much interest in the role of apolipoprotein E (apoE) genotype in late-onset Alzheimer's disease, and examination of this question involves the genotyping of large groups of cases. 1,2 Many of the studies have used the method of apoE genotyping described by Hixson and Vernier 3, which has the advantage of using a single restriction enzyme to identify two polymorphic sites. However, this method involves the separation of relatively small fragments (72, 83, and 91 bp) of DNA, necessitating the use of large polyacrylamide gels that need more expensive equipment and are more technically demanding than agarose gels. This is especially relevant when there is need to screen hundreds of dementia patients for apoE genotype. Furthermore, even when the assays are done by well-equipped laboratories, the results are sometimes ambiguous 4, and although the use of radioactive reagents may improve the quality of …
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
Differences in Age-related Retinal and Cortical Atrophy Rates in Multiple Sclerosis
Prof. Massimo Filippi and Dr. Paolo Preziosa
► Watch
Related Articles
- No related articles found.
Alert Me
Recommended articles
-
ARTICLES
ApoE and CYP2D6 polymorphism with and without parkinsonism-dementia complex in the people of Chamorro, GuamX. Chen, Y. Xia, L. S. Gresham et al.Neurology, September 01, 1996 -
Articles
Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob diseaseJ.A. Mastrianni, C. Iannicola, R.M. Myers et al.Neurology, November 01, 1996 -
Articles
Polymorphism of the prion protein is associated with cognitive impairment in the elderlyThe EVA studyC. Berr, F. Richard, C. Dufouil et al.Neurology, September 01, 1998 -
Brief Communications
A mitochondrial tRNAVal gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI. F. M. de Coo, E. A. Sistermans, I. J. de Wijs et al.Neurology, January 01, 1998