Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene

1 Jun 1992

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alzheimer's disease research and treatments
Share to Amyloidosis: Diagnosis, Treatment, Outcomes
Share to Prion Diseases and Protein Misfolding

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 1303239
DOI: 10.1038/ng0692-218

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein genePMID 1303239Read ↗

Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692).Semantic proximity Read ↗

TARDBP mutation p.Ile383Val associated with semantic dementia and complex proteinopathy.Semantic proximity Read ↗

Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutation.Semantic proximity Read ↗

Presenilin-2 gene mutation presenting as Lewy body dementia?Semantic proximity Read ↗

Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.Semantic proximity Read ↗

Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.Semantic proximity Read ↗

[From gene to disease; amyloid-beta precursor protein gene instrumental in hereditary cerebral amyloid angiopathies].Semantic proximity Read ↗

Presenilin1 G217R mutation linked to Alzheimer disease with cotton wool plaques.Semantic proximity Read ↗

Mutation in codon 713 of the β amyloid precursor protein gene presenting with schizophreniaSemantic proximity Read ↗

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage.Semantic proximity Read ↗

Amyloid β in hereditary cerebral hemorrhage with amyloidosis-Dutch type.Semantic proximity Read ↗

A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.