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

Mutations analysis of RAB39B gene in Chinese early-onset Parkinson's disease.

Parkinsonism & related disorders - 1 Jul 2016

Liu Zhenhua, Tang Beisha, Guo Jifeng, Zhou Xiaoxia, Sun Qiying, Xu Qian, Xu Changshui, Yan Xinxiang

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 Age of Onset
Share to Asian People
Share to DNA Mutational Analysis
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Parkinson Disease

Share to rab GTP-Binding Proteins

Source

Identifiers

PMID: 27036214
DOI: 10.1016/j.parkreldis.2016.03.019

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations analysis of RAB39B gene in Chinese early-onset Parkinson's disease.PMID 27036214Read ↗

Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.Semantic proximity Read ↗

Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease.Semantic proximity Read ↗

RAB39B gene mutations are not linked to familial Parkinson's disease in China.Semantic proximity Read ↗

RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies.Semantic proximity Read ↗

Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein PathologySemantic proximity Read ↗

A novel RAB39B gene mutation in X‐linked juvenile parkinsonism with basal ganglia calcificationSemantic proximity Read ↗

Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's Disease.Semantic proximity Read ↗

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.Semantic proximity Read ↗

Novel RAB39B variant associated intellectual disability and levodopa-responsive young-onset parkinsonism.Semantic proximity Read ↗

The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease.Semantic proximity Read ↗

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosisSemantic proximity Read ↗

LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population.Semantic proximity Read ↗

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