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

Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia.

Neurobiology of aging - 1 Oct 2016

Tang Min, Gu Xiaohua, Wei Jingya, Jiao Bin, Zhou Lin, Zhou Yafang, Weng Ling, Yan Xinxiang, Tang Beisha, Xu Jun, Shen Lu

Abstract excerpt

Frontotemporal dementia (FTD) is a clinically heterogeneous neurodegenerative disorder, including behavior behavioral variant FTD (bvFTD), semantic dementia, progressive nonfluent aphasia (PNFA), FTD-parkinsonism, and FTD-motor neuron disease. To date, there are at least 8 causative genes identified in patients with FTD. Among them, variants in the microtubule-associated protein tau (MAPT), GRN, and chromosome 9...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to C9orf72 Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Frontotemporal Dementia

Share to Genetic Association Studies

Share to Intercellular Signaling Peptides and Proteins

Share to Progranulins

Share to Proteins

Share to tau Proteins

Source

Identifiers

PMID: 27311648
DOI: 10.1016/j.neurobiolaging.2016.05.013

Genes

MAPT
GRN

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia.PMID 27311648Read ↗

Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia.Semantic proximity Read ↗

Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population.Semantic proximity Read ↗

Genetic Features of MAPT, GRN, C9orf72 and CHCHD10 Gene Mutations in Chinese Patients with Frontotemporal Dementia.Semantic proximity Read ↗

Genetics of frontotemporal dementia in China.Semantic proximity Read ↗

Identification and functional characterization of novel variants of MAPT and GRN in Chinese patients with frontotemporal dementia.Semantic proximity Read ↗

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS.Semantic proximity Read ↗

Genetic Spectrum and Clinical Heterogeneity of Chinese Frontotemporal Dementia Patients: Data from PUMCH Dementia Cohort.Semantic proximity Read ↗

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.Semantic proximity Read ↗

Phenotype Heterogeneity and Genotype Correlation of MAPT Mutations in a Chinese PUMCH Cohort.Semantic proximity Read ↗

GRN and MAPT Mutations in 2 Frontotemporal Dementia Research Centers in Brazil.Semantic proximity Read ↗

The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han PatientsSemantic proximity Read ↗

Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients.Semantic proximity Read ↗

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