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

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.

Arquivos de neuro-psiquiatria - 1 Sept 2001

Teive H A, Raskin S, Iwamoto F M, Germiniani F M, Baran M H, Werneck L C, Allan N, Quagliato E, Leroy E, Ide S E, Polymeropoulos M H

Abstract excerpt

A missense G209A mutation of the alpha-synuclein gene was recently described in a large Contursi kindred with Parkinson's disease (PD). The objective of this study is to determine if the mutation G209A of the alpha-synuclein gene was present in 10 Brazilian families with PD. PD patients were recruited from movement disorders clinics of Brazil. A family history with two or more affected in relatives was the...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to alpha-Synuclein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Brazil

Share to Nerve Tissue Proteins

Share to Parkinson Disease

Share to Pedigree

Share to Restriction Mapping

Share to Synucleins

Source

Identifiers

PMID: 11593272
DOI: 10.1590/s0004-282x2001000500013

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

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.PMID 11593272Read ↗

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

Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.Semantic proximity Read ↗

Mutated alpha-synuclein gene in two Greek kindreds with familial PD: incomplete penetrance?Semantic proximity Read ↗

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

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.Semantic proximity Read ↗

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

Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation.Semantic proximity Read ↗

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.Semantic proximity Read ↗

Alpha-synuclein A53T mutation is not frequent on a sample of Brazilian Parkinson's disease patients.Semantic proximity Read ↗

Alpha‐synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patientsSemantic proximity Read ↗

Dementia with Lewy bodies in an elderly Greek male due to alpha-synuclein gene mutation.Semantic proximity Read ↗

The alpha-synuclein gene and Parkinson disease in a Chinese population.Semantic proximity Read ↗

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