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

LRP10 in autosomal‐dominant Parkinson's disease

9 Apr 2019

Abstract excerpt

BACKGROUND: Recently, the LRP10 gene has been identified as a novel genetic cause in individuals affected by Parkinson's disease (PD), Parkinson's disease dementia, or dementia with Lewy bodies. OBJECTIVE: We investigated the involvement of LRP10 mutations in Chinese patients with familial PD and reviewed previous studies of LRP10 mutations in patients with PD. METHODS: A mutation analysis of the LRP10 gene was...

Read the complete abstract on PubMed

Topics

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

Share to Lysosomal Storage Disorders Research
Share to Neurological diseases and metabolism
Share to Parkinson's Disease Mechanisms and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30964957
DOI: 10.1002/mds.27693

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

LRP10 in autosomal‐dominant Parkinson's diseasePMID 30964957Read ↗

LRP10 Mutations May Correlate with Sporadic Parkinson's Disease in China.Semantic proximity Read ↗

Genetic analysis of the LRP10 gene in Chinese patients with Parkinson's disease.Semantic proximity Read ↗

Mutation analysis of LRP10 in a large Chinese familial Parkinson disease cohort.Semantic proximity Read ↗

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing studySemantic proximity Read ↗

Rare, pathogenic variants in LRP10 are associated with amyotrophic lateral sclerosis in patients from mainland China.Semantic proximity Read ↗

Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy.Semantic proximity Read ↗

Clinical and Pathological Phenotypes of LRP10 Variant Carriers with Dementia.Semantic proximity Read ↗

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.Semantic proximity Read ↗

Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease.Semantic proximity Read ↗

The LRRK2 gene is mutated in a Chinese autosomal-dominant Parkinson's disease family.Semantic proximity Read ↗

LRP10 variants in progressive supranuclear palsy.Semantic proximity Read ↗

Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact.Semantic proximity Read ↗

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