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

Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease.

Neurobiology of aging - 1 May 2017

Rubino Elisa, Brusa Livia, Zhang Ming, Boschi Silvia, Govone Flora, Vacca Alessandro, Gai Annalisa, Pinessi Lorenzo, Lopiano Leonardo, Rogaeva Ekaterina, Rainero Innocenzo

Abstract excerpt

In recent years, CHCHD2 and CHCHD10 mutations were reported to be associated with a broad spectrum of neurodegenerative diseases, including Parkinson's disease (PD), although with conflicting results in different populations. The present study aimed to evaluate CHCHD2 and CHCHD10 coding variants in Italian patients with PD. All the coding regions and flanking intronic splice sites of CHCHD2 and CHCHD10 were...

Read the complete abstract on PubMed

Topics

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

Share to Cohort Studies
Share to DNA-Binding Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Introns

Share to Mitochondria

Share to Mitochondrial Proteins

Share to Parkinson Disease

Source

Identifiers

PMID: 28108040
DOI: 10.1016/j.neurobiolaging.2016.12.027

Genes

CHCHD2
CHCHD10

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

Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease.PMID 28108040Read ↗

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.Semantic proximity Read ↗

Genetic analysis of CHCHD2 in a southern Spanish population.Semantic proximity Read ↗

Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease.Semantic proximity Read ↗

Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.Semantic proximity Read ↗

Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria.Semantic proximity Read ↗

Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literature.Semantic proximity Read ↗

Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy.Semantic proximity Read ↗

CHCHD2 gene mutations in familial and sporadic Parkinson's disease.Semantic proximity Read ↗

A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease.Semantic proximity Read ↗

CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61ISemantic proximity Read ↗

Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population.Semantic proximity Read ↗

Mutation Screening of the CHCHD2 Gene for Alzheimer's Disease and Frontotemporal Dementia in Chinese Mainland Population.Semantic proximity Read ↗

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