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

Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease

2 Aug 2013

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Genomics and Rare Diseases
Share to Nuclear Receptors and Signaling
Share to Parkinson's Disease Mechanisms and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23916651
DOI: 10.1016/j.parkreldis.2013.07.011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's diseasePMID 23916651Read ↗

Analysis of the α-synuclein G209A mutation in familial Parkinson's diseaseSemantic proximity Read ↗

Phenotypic spectrum of alpha-synuclein mutations: New insights from patients and cellular models.Semantic proximity Read ↗

AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseSemantic proximity Read ↗

Absence of the G209A mutation in the alpha-synuclein gene in British families with Parkinson's disease.Semantic proximity Read ↗

Update on novel familial forms of Parkinson's disease and multiple system atrophy.Semantic proximity Read ↗

Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: a meta-analysis.Semantic proximity Read ↗

Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.Semantic proximity Read ↗

SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.Semantic proximity Read ↗

Genetic Analysis and Literature Review of SNCA Variants in Parkinson's DiseaseSemantic proximity Read ↗

Genetics of synucleins in neurodegenerative diseasesSemantic proximity Read ↗

Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseasesSemantic proximity Read ↗

Absence of SNCA polymorphisms in Pakistani Parkinsons disease patients.Semantic proximity Read ↗

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