Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease
<p>Abstract</p> <p>Background</p> <p>Mitochondrial function is impaired in Parkinson's disease (PD) and may contribute to the pathogenesis of PD, but the causes of mitochondrial impairment in PD are unknown. Mitochondrial dysfunction is recapitulated in cell lines...
Saved in:
Main Authors: | Pfeiffer Ronald F (Author), Rudolph Alice (Author), Halter Cheryl A (Author), Pauciulo Michael W (Author), Kissell Diane K (Author), Pankratz Nathan (Author), Simon David K (Author), Nichols William C (Author), Foroud Tatiana (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2010-04-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Genomewide association study for onset age in Parkinson disease
by: Halter Cheryl, et al.
Published: (2009) -
Genotype-Phenotype Correlation of Maternally Inherited Disorders due to Mutations in Mitochondrial DNA
by: Peterus Thajeb, et al.
Published: (2006) -
Evidence of hybridization, mitochondrial introgression and biparental inheritance of the kDNA minicircles in Trypanosoma cruzi I.
by: Fanny Rusman, et al.
Published: (2020) -
Mitochondrial DNA 7908-8816 region mutations in maternally inherited essential hypertensive subjects in China
by: Ye Zhu, et al.
Published: (2018) -
Associations of mitochondrial DNA 3777-4679 region mutations with maternally inherited essential hypertensive subjects in China
by: Ye Zhu, et al.
Published: (2020)