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

Mutation analysis of the GLA gene in Chinese patients with intracerebral hemorrhage.

Neurobiology of aging - 1 Jun 2021

Tang Lu, Yang Qiong, Liu Xiaolu, Tian Danyang, Wu Chenying, Han Qi, Yan Xin, Ding Shengchao, Fan Dongsheng

Abstract excerpt

Fabry disease (FD) is an important underlying condition in young cryptogenic stroke patients and has also been implicated in cerebral small vessel disease. However, the contributions of causative GLA mutations in patients with intracerebral hemorrhage (ICH) remain unclear. In this study, GLA sequences were analyzed in a Chinese ICH cohort comprising 373 patients with computed tomography-confirmed ICH and 563...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Galactosidase
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cohort Studies

Share to DNA Mutational Analysis

Share to Fabry Disease

Share to Genetic Association Studies

Share to Sex Characteristics

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 33663879
DOI: 10.1016/j.neurobiolaging.2021.01.027

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation analysis of the GLA gene in Chinese patients with intracerebral hemorrhage.PMID 33663879Read ↗

Screening for Fabry's disease in young patients with ischemic stroke in a Chinese population.Semantic proximity Read ↗

Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients.Semantic proximity Read ↗

Prevalence of Fabry disease and GLA variants in young patients with acute stroke: The challenge to widen the screening. The Fabry-Stroke Italian Registry.Semantic proximity Read ↗

Genomic screening of Fabry disease in young stroke patients: the Taiwan experience and a review of the literatureSemantic proximity Read ↗

Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants.Semantic proximity Read ↗

Mutations of the <i>GLA</i> Gene in Young Patients With StrokeSemantic proximity Read ↗

[Prevalence of ischemic stroke in young adults and Fabry disease].Semantic proximity Read ↗

High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry.Semantic proximity Read ↗

Fabry disease: GLA deletion alters a canonical splice site in a family with neuropsychiatric manifestations.Semantic proximity Read ↗

p.R220L Is a Likely Pathogenic Novel GLA Gene Mutation Responsible for Fabry Disease.Semantic proximity Read ↗

Genetic characteristics of Chinese patients with hemorrhagic cerebrovascular disease.Semantic proximity Read ↗

p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males.Semantic proximity Read ↗

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