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NEUROLOGY 1996;46:1156-1157
© 1996 American Academy of Neurology

Normal distribution of apolipoprotein E alleles in progressive supranuclear palsy

A. Anouti, MD, K. Schmidt, BS, K. E. Lyons, PhD, J. P. Hubble, MD, G. Schellenberg, PhD, L. I. Golbe, MD, A. E. Lang, MD, N. Galvez-Jimenez, MD, L. Hershey, MD, PhD and W.C. Koller, MD, PhD

From the Department of Neurology (Drs. Anouti, Lyons, Hubble, and Koller, and K. Schmidt), University of Kansas Medical Center, Kansas City, KS; the Gerontology Research Education and Clinical Center (Dr. Schellenberg), Seattle Veterans Affairs Medical Center, Seattle, WA; the Department of Neurology (Dr. Golbe), UMDNJ-Robert Wood Johnson Medical School, New Brunswick, NJ; the Division of Neurology (Drs. Lang and Galvez-Jimenez), The Toronto Hospital, 339 Bathurst Street MP11-304, Toronto, Canada; and the Neurology Service (Dr. Hershey), Buffalo Veterans Affairs Medical Center, Buffalo, NY.
Received June 22, 1995. Accepted in final form September 19, 1995.
Address correspondence and reprint requests to Dr. William C. Koller, Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Blvd, Kansas City, KS 66160-7314.

Apolipoprotein E (Apo E) genotype is a genetic risk factor influencing the development of Alzheimer's disease (AD).Progressive supranuclear palsy (PSP), like AD, is a dementing illness with neurofibrillary tangles. We determined the frequencies of Apo E alleles in 52 PSP patients and 52 age- and gender-matched controls. The distribution of Apo E allele frequencies and genotypes showed no difference between PSP and controls. Apo E allele status does not influence the development of PSP.

NEUROLOGY 1996;46: 1156-1157




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