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

CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61I

23 Oct 2018

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 Genetic Neurodegenerative Diseases
Share to Genetics and Neurodevelopmental Disorders
Share to Parkinson's Disease Mechanisms and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30530185
DOI: 10.1016/j.neurobiolaging.2018.10.020

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61IPMID 30530185Read ↗

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing studySemantic proximity Read ↗

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

Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10–what distinguishes the two?Semantic proximity Read ↗

A nonsense mutation in CHCHD2 in a patient with Parkinson disease.Semantic proximity Read ↗

CHCHD2 p. Thr61Ile knock‐in mice exhibit motor defects and neuropathological features of Parkinson's diseaseSemantic proximity Read ↗

CHCHD2 and CHCHD10-related neurodegeneration: molecular pathogenesis and the path to precision therapy.Semantic proximity Read ↗

Mutation analysis of<i>CHCHD10</i>in different neurodegenerative diseasesSemantic proximity Read ↗

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

CHCHD2 and Parkinson's diseaseSemantic proximity Read ↗

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

Mitochondrial CHCHD2 and CHCHD10: Roles in Neurological Diseases and Therapeutic ImplicationsSemantic proximity Read ↗

CHCHD2 links mitochondrial dysfunction and α-synuclein misfolding in Parkinson's disease.Semantic proximity Read ↗

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