Mutations of mitochondrial DNA (mtDNA) are frequent in humans and are implicated in many different types of pathology. The high substitution rate and the maternal, asexual mode of transmission of mtDNA make it more likely to accumulate deleterious mutations. Here, we discuss recent evidence that mtDNA transmission is subject to strong purifying selection in the mammalian female germ line, limiting the accumulation of such mutations. This process shapes mitochondrial sequence diversity and is therefore probably of fundamental importance for animal evolution and in human mitochondrial disease
Item does not contain fulltextThe peculiar biology of mitochondrial DNA (mtDNA) potentially has detr...
Mitochondrial DNA (mtDNA), the circular DNA molecule inside the mitochondria of all eukaryotic cells...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
There is an intense debate concerning whether selection or demographics has been most important in s...
There is an intense debate concerning whether selection or demographics has been most important in s...
Inherited mutations in the mitochondrial (mt)DNA are a major cause of human disease, with approximat...
The peculiar biology of mitochondrial DNA (mtDNA) potentially has detrimental consequences for organ...
Abstract Mitochondrial DNA (mtDNA) is a maternally inherited 16.6 kbp circular genome that codes for...
The peculiar biology of mitochondrial DNA (mtDNA) potentially has detrimental consequences for organ...
The peculiar biology of mitochondrial DNA (mtDNA) potentially has detrimental consequences for organ...
Common genetic variants of mitochondrial DNA (mtDNA) increase the risk of developing several of the ...
Since the unexpected discovery that mitochondria contain their own distinct DNA molecules, studies o...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Since the unexpected discovery that mitochondria contain their own distinct DNA molecules, studies o...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Item does not contain fulltextThe peculiar biology of mitochondrial DNA (mtDNA) potentially has detr...
Mitochondrial DNA (mtDNA), the circular DNA molecule inside the mitochondria of all eukaryotic cells...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
There is an intense debate concerning whether selection or demographics has been most important in s...
There is an intense debate concerning whether selection or demographics has been most important in s...
Inherited mutations in the mitochondrial (mt)DNA are a major cause of human disease, with approximat...
The peculiar biology of mitochondrial DNA (mtDNA) potentially has detrimental consequences for organ...
Abstract Mitochondrial DNA (mtDNA) is a maternally inherited 16.6 kbp circular genome that codes for...
The peculiar biology of mitochondrial DNA (mtDNA) potentially has detrimental consequences for organ...
The peculiar biology of mitochondrial DNA (mtDNA) potentially has detrimental consequences for organ...
Common genetic variants of mitochondrial DNA (mtDNA) increase the risk of developing several of the ...
Since the unexpected discovery that mitochondria contain their own distinct DNA molecules, studies o...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Since the unexpected discovery that mitochondria contain their own distinct DNA molecules, studies o...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Item does not contain fulltextThe peculiar biology of mitochondrial DNA (mtDNA) potentially has detr...
Mitochondrial DNA (mtDNA), the circular DNA molecule inside the mitochondria of all eukaryotic cells...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...