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September 01, 1994; 44 (9) Articles

The risk of developing Creutzfeldt‐Jakob disease in subjects with the PRNP gene codon 200 point mutation

Joab Chapman, Joshua Ben-Israel, Yochanan Goldhammer, Amos D. Korczyn
First published September 1, 1994, DOI: https://doi.org/10.1212/WNL.44.9.1683
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Article Information

vol. 44 no. 9 1683
DOI: 
https://doi.org/10.1212/WNL.44.9.1683
PubMed: 
7936296
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published September 1, 1994.
Copyright & Usage: 
© 1994 by the American Academy of Neurology

Author Disclosures

    1. Joab Chapman, MD, PhD,
    2. Joshua Ben-Israel, MD,
    3. Yochanan Goldhammer, MD and
    4. Amos D. Korczyn, MD, MSc
  1. Joab Chapman, MD, PhD,
  2. Joshua Ben-Israel, MD,
  3. Yochanan Goldhammer, MD and
  4. Amos D. Korczyn, MD, MSc
  1. Departments of Neurology, Tel Aviv Medical Center (Drs. Chapman and Korczyn) and Sheba Medical Center (Dr. Goldhammer), Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel; and Medical Geriatric Center (Dr. Ben-Israel), Nethanya, Israel.

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