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

A 57-Year-Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations.

Annals of clinical and translational neurology - 1 Aug 2026

Lin Feifei, Huang Saie

Abstract excerpt

This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its clinical manifestations, neuropsychological assessments, cerebrospinal...

Topics

Join the communities discussing this publication.

Frontotemporal Dementia
NOS3 gene
Mutation
Nitric Oxide Synthase Type III
RNA-Binding Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 42374607
DOI: 10.1002/acn3.70459
PMCID: PMC13394904

Genes

MATR3
NOS3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A 57-Year-Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations.PMID 42374607Read ↗

Behavioral variant frontotemporal dementia associated with GRN and ErbB4 gene mutations: a case report and literature review.Semantic proximity Read ↗

Clinical and molecular aspects of frontotemporal dementia.Semantic proximity Read ↗

Behavioral variant frontotemporal dementia associated with a NEK1 missense variant: exploring a possible phenotypic association.Semantic proximity Read ↗

Behavioural Variant Frontotemporal Dementia due to CCNF Gene Mutation: A Case Report.Semantic proximity Read ↗

Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations.Semantic proximity Read ↗

Behavioral variant of frontotemporal dementia in carriers of biallelic TREM2 variants: cases study.Semantic proximity Read ↗

Very early-onset behavioral variant frontotemporal dementia in a patient with a variant of uncertain significance of a FUS gene mutation.Semantic proximity Read ↗

Slowly progressive behavioral frontotemporal dementia with C9orf72 mutation. Case report and review of the literature.Semantic proximity Read ↗

A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathy.Semantic proximity Read ↗

Identification of rare RTN3 variants in Alzheimer's disease in Han Chinese.Semantic proximity Read ↗

CADASIL presenting with a behavioural variant frontotemporal dementia phenotype.Semantic proximity Read ↗

Neuroimaging features in C9orf72 and TARDBP double mutation with FTD phenotype.Semantic proximity Read ↗

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