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

Effects of PRRT2 mutation on brain gray matter networks in paroxysmal kinesigenic dyskinesia.

Cerebral cortex (New York, N.Y. : 1991) - 14 Jan 2024

Li Xiuli, Lei Du, Qin Kun, Li Lei, Zhang Yingying, Zhou Dong, Kemp Graham J, Gong Qiyong

Abstract excerpt

Although proline-rich transmembrane protein 2 is the primary causative gene of paroxysmal kinesigenic dyskinesia, its effects on the brain structure of paroxysmal kinesigenic dyskinesia patients are not yet clear. Here, we explored the influence of proline-rich transmembrane protein 2 mutations on similarity-based gray matter morphological networks in individuals with paroxysmal kinesigenic dyskinesia. A total of...

Read the complete abstract on PubMed

Topics

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

Share to Brain
Share to Dystonia
Share to Gray Matter

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Mutation

Share to Nerve Tissue Proteins

Source

Identifiers

PMID: 37955636
DOI: 10.1093/cercor/bhad418

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

Effects of PRRT2 mutation on brain gray matter networks in paroxysmal kinesigenic dyskinesia.PMID 37955636Read ↗

Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.Semantic proximity Read ↗

Motor-planning cerebello-cerebral network alterations in PRRT2-related paroxysmal kinesigenic dyskinesia.Semantic proximity Read ↗

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.Semantic proximity Read ↗

Motor Functional Hierarchical Organization of Cerebrum and Its Underlying Genetic Architecture in Parkinson’s DiseaseSemantic proximity Read ↗

PRRT2 mutations and paroxysmal disorders.Semantic proximity Read ↗

Disrupted topological properties of structural brain networks present a glutamatergic neuropathophysiology in people with narcolepsySemantic proximity Read ↗

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.Semantic proximity Read ↗

Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A Variants.Semantic proximity Read ↗

Disrupted topological organization of resting-state functional brain networks in Parkinson's disease patients with glucocerebrosidase gene mutations.Semantic proximity Read ↗

<i>BCKDK</i>rs14235 A allele is associated with milder motor impairment and altered network topology in Parkinson’s diseaseSemantic proximity Read ↗

Identifying a Whole-brain Connectome-based Model in Drug-naïve Parkinson’s Disease for Predicting Motor ImpairmentSemantic proximity Read ↗

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study.Semantic proximity Read ↗

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