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Molecular Genetics of Familial Alzheimer's Disease

Published online by Cambridge University Press:  18 September 2015

P.H. George-Hyslop*
Affiliation:
Molecular Neurogenetics Laboratory, Research 3, Massachusetts General Hospital, Boston
J.L. Haines
Affiliation:
Molecular Neurogenetics Laboratory, Research 3, Massachusetts General Hospital, Boston
R.J. Polinsky
Affiliation:
Neuropharmacology Division, Medical Neurology Branch, NINCDS, Bethesda
R.E. Tanzi
Affiliation:
Molecular Neurogenetics Laboratory, Research 3, Massachusetts General Hospital, Boston
L. Farrer
Affiliation:
Neurogenetics Laboratory and School of Medicine, Boston University School of Medicine, Boston
R.H. Myers
Affiliation:
Neurogenetics Laboratory and School of Medicine, Boston University School of Medicine, Boston
J.F. Gusella
Affiliation:
Molecular Neurogenetics Laboratory, Research 3, Massachusetts General Hospital, Boston
*
Molecular Neurogenetics Lab, Research 3, Massachusetts General Hospital, 32 Fruit St., Boston MA, U.S.A. 02114
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Abstract:

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The molecular genetic strategies aimed at isolating and characterizing the defective gene(s) in familial Alzheimer's disease, the inherent limitations of the techniques and recent progress in the field are reviewed. Three independent groups have found an apparent linkage to chromosome 21 but two other groups have not, suggesting that familial Alzheimer's disease may be etiologically heterogeneous.

Type
Research Article
Copyright
Copyright © Canadian Neurological Sciences Federation 1989

References

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