📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

The presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aß43 and atypical clinical manifestations (2024)

First Author: Arber C

Attributed to: UKDP: Integrated DEmentiA research environment (IDEA) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/alz.13904

Publication URI: http://dx.doi.org/10.1002/alz.13904

Type: Journal Article/Review

Parent Publication: Alzheimer's & Dementia

Issue: 7

ISSN: 1552-5260