A mutation in the Amyloid Precursor Protein Associated with Hereditary Alzheimer's Disease-Reference-Cited by-同舟云学术

A mutation in the Amyloid Precursor Protein Associated with Hereditary Alzheimer's Disease

Published:1991-10-04 Issue:5028 Volume:254 Page:97-99
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Murrell Jill¹,Farlow Martin¹,Ghetti Bernardino¹,Benson Merrill D.¹

Affiliation:

1. Indiana University School of Medicine, Departments of Medicine, Medical and Molecular Genetics, Neurology, Pathology, and the Veterans Affairs Richard L. Roudebush Medical Center Indianapolis, IN 46202.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference28 articles.

1. Benson M. D. The Metabolic Basis of Inherited Disease 6: 2439 (1989).

2. Christmanson, L., Amyloid and Amyloidosis: 635 (1990).

3. DOHURA, K, PRO-]LEU CHANGE AT POSITION-102 OF PRION PROTEIN IS THE MOST COMMON BUT NOT THE SOLE MUTATION RELATED TO GERSTMANN-STRAUSSLER SYNDROME, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 163: 974 (1989).

4. GHISO, J, AMYLOID FIBRILS IN HEREDITARY CEREBRAL-HEMORRHAGE WITH AMYLOIDOSIS OF ICELANDIC TYPE IS A VARIANT OF GAMMA-TRACE BASIC-PROTEIN (CYSTATIN-C), PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 83: 2974 (1986).

5. GLENNER, G.G., ALZHEIMERS-DISEASE - INITIAL REPORT OF THE PURIFICATION AND CHARACTERIZATION OF A NOVEL CEREBROVASCULAR AMYLOID PROTEIN, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 120: 885 (1984).

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