A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of A 42(43)-Reference-Cited by-同舟云学术

A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of A 42(43)

Published:1997-11-01 Issue:12 Volume:6 Page:2087-2089
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Eckman C. B.,Mehta N. D.,Crook R.,Perez-tur J.,Prihar G.,Pfeiffer E.,Graff-Radford N.,Hinder P.,Yager D.,Zenk B.,Refolo L. M.,Mihail Prada C.,Younkin S. G.,Hutton M.,Hardy J.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/6/12/2087/6953658/6-12-2087.pdf

Reference12 articles.

1. Amyloid, the presenilins and Alzheimer's disease

2. Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease

3. Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1

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