Rare mutations in the mitochondrial protein coiled-coil-helix-coiled-coil-helix domain
containing 2 (CHCHD2) are associated with Parkinson's disease (PD) and other Lewy body …

Twenty-five years have passed since the causative gene for familial Parkinson's disease
(PD), Parkin (now PRKN), was identified in 1998; PRKN is the most common causative gene …

Mutations in CHCHD2 are linked to a familial, autosomal dominant form of Parkinson's
disease (PD). The gene product may regulate mitochondrial respiratory function. However …

Abstract Coiled-coil-helix-coiled-coil-helix domain containing protein 2 (CHCHD2) mutations
were linked with autosomal dominant Parkinson's disease (PD) and recently, Alzheimer's …

Coiled-coil-helix-coiled-coil-helix domain containing 2 (CHCHD2) and Coiled-coil-helix-
coiled-coil-helix domain containing 10 (CHCHD10) are mitochondrial proteins that are …

Mutations of coiled-coil-helix-coiled-coil-helix domain containing 2 (CHCHD2) and 10
(CHCHD10) have been found to be linked to Parkinson's disease (PD), amyotrophic lateral …

Multiple system atrophy (MSA) is a rare neurodegenerative disease characterized by
parkinsonism, cerebellar impairment, and autonomic failure. Although the causes of MSA …

α-Synuclein (αSyn) plays a major role in the pathogenesis of Parkinson's disease (PD),
which is the second most common neurodegenerative disease after Alzheimer's disease …

Multiple system atrophy (MSA) is a devastating neurodegenerative disease characterized by
the clinical triad of parkinsonism, cerebellar ataxia and autonomic failure, impacting on …

CHCHD2 mutations have been identified in various neurological diseases such as
Parkinson's disease (PD), frontotemporal dementia (FTD), and Alzheimer's disease (AD). It …