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

DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.

Parkinsonism & related disorders - 1 Oct 2018

Gagliardi Monica, Annesi Grazia, Procopio Radha, Morelli Maurizio, Iannello Grazia, Bonapace Giuseppe, Mancini Manuela, Nicoletti Giuseppe, Quattrone Aldo

Abstract excerpt

BACKGROUND: Parkinson's disease (PD) is the second most common neurodegenerative disorder, and the most common neurodegenerative form of parkinsonism. Recently, a pathogenic mutation (p.N855S) in DNAJC13 was linked to autosomal dominant Lewy body PD in a Dutch-German-Russian Mennonite multi-incident kindred, and was found in five additional patients. In this study, we performed a comprehensive screening of the...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to HSP40 Heat-Shock Proteins

Share to Mutation

Share to Parkinson Disease

Source

Identifiers

PMID: 29887357
DOI: 10.1016/j.parkreldis.2018.06.004

Genes

DNAJC13

Variants

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

DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.PMID 29887357Read ↗

DNAJC13 genetic variants in parkinsonism.Semantic proximity Read ↗

Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.Semantic proximity Read ↗

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.Semantic proximity Read ↗

Variants in <i>DNAJC13</i> Are Not Associated with Parkinson’s Disease Across Different Ancestral BackgroundsSemantic proximity Read ↗

Clinical, positron emission tomography, and pathological studies of DNAJC13 p.N855S Parkinsonism.Semantic proximity Read ↗

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls.Semantic proximity Read ↗

The genetic associations of DNAJC family members with Parkinson's disease: comprehensive evidence from burden analysis and Mendelian randomization.Semantic proximity Read ↗

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.Semantic proximity Read ↗

DNAJC6 mutations are not common causes of early onset Parkinson's disease in Chinese Han population.Semantic proximity Read ↗

Genetic Analysis of Patients With Early-Onset Parkinson’s Disease in Eastern ChinaSemantic proximity Read ↗

DNAJC13 mutations in Parkinson disease.Semantic proximity Read ↗

DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease.Semantic proximity Read ↗

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