# A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/a-pathogenic-mutation-for-probable-alzheimer-s-disease-in-the-app-gene-at-the-n/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Mike Mullan,Fiona Crawford,Karin Axelman,Henry Houlden,Lena Lilius,Bengt Winblad,Lars Lannfelt |
| Citations | 1,511 |
| DOI | 10.1038/ng0892-345 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2030641075 |
| PMID | 1302033 |
| Type | article |
| Year | 1992 |

## Paper authors

- [Bengt Winblad](https://scholariq.org/researchers/bengt-winblad/)

## Paper primary topic

- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)

## Paper topics

- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Amyloidosis: Diagnosis, Treatment, Outcomes](https://scholariq.org/topics/amyloidosis-diagnosis-treatment-outcomes/)
- [Prion Diseases and Protein Misfolding](https://scholariq.org/topics/prion-diseases-and-protein-misfolding/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.