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

[Association between mutations of SCN9A gene and pain related to Parkinsonism].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Feb 2013

Zhang Li-mei, Chen Yong-qian, Li Wan-jun, Sun Wei, Huang Yue, Zou Hai-qiang

Abstract excerpt

OBJECTIVE: To screening mutations of exons 15, 18 and 26 of sodium channel Nav1.7 (SCN9A) gene, and to assess its association with pain related to Parkinsonism. METHODS: Respectively, 101 patients with primary Parkinson's disease (PD) and 104 similar-aged volunteers without PD were recruited from March, 2008 to January, 2011. Mutations of above 3 exons in SCN9A gene was detected with PCR and direct sequencing....

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Base Sequence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to NAV1.7 Voltage-Gated Sodium Channel

Share to Parkinson Disease

Share to Prevalence

Source

Identifiers

PMID: 23450472
DOI: 10.3760/cma.j.issn.1003-9406.2013.01.005

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

[Association between mutations of SCN9A gene and pain related to Parkinsonism].PMID 23450472Read ↗

Contribution of genetic variants to pain susceptibility in Parkinson disease.Semantic proximity Read ↗

[Neuropathic pain associated with Nav1.7 mutations: clinical picture and treatment].Semantic proximity Read ↗

Pain in Parkinson's disease associated with COMT gene polymorphisms.Semantic proximity Read ↗

Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels.Semantic proximity Read ↗

Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease.Semantic proximity Read ↗

Chronic Pain in Parkinson’s Disease: Prevalence, Sex Differences, Regional Anatomy and ComorbiditiesSemantic proximity Read ↗

Pain in SCN4A Mutated P.A1156T muscle sodium channelopathy-a postal survey.Semantic proximity Read ↗

Pain in Parkinson disease: a deep phenotyping study.Semantic proximity Read ↗

Prevalence of pain phenotypes and co-morbidities of chronic pain in Parkinson's Disease.Semantic proximity Read ↗

Association between MMP16 rs60298754 and clinical phenotypes of Parkinson's disease in southern Chinese.Semantic proximity Read ↗

[Association of the polymorphisms in NURR1 gene with Parkinson's disease].Semantic proximity Read ↗

Contribution of functional dopamine D2 and D3 receptor variants to motor and non-motor symptoms of early onset Parkinson's disease.Semantic proximity Read ↗

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