textabstractAlthough previous studies have documented a bottleneck in the transmission of mtDNA genomes from mothers to offspring, several aspects remain unclear, including the size and nature of the bottleneck. Here, we analyze the dynamics of mtDNA heteroplasmy transmission in the Genomes of the Netherlands (GoNL) data, which consists of complete mtDNA genome sequences from 228 trios, eight dizygotic (DZ) twin quartets, and 10 monozygotic (MZ) twin quartets. Using a minor allele frequency (MAF) threshold of 2%, we identified 189 heteroplasmies in the trio mothers, of which 59% were transmitted to offspring, and 159 heteroplasmies in the trio offspring, of which 70% were inherited from the mothers. MZ twin pairs exhibited greater similarit...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
Common genetic variants of mitochondrial DNA (mtDNA) increase the risk of developing several of the ...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...
Although previous studies have documented a bottleneck in the transmission of mtDNA genomes from mot...
Although previous studies have documented a bottleneck in the transmission of mtDNA genomes from mot...
Although previous studies have documented a bottleneck in the transmission of mtDNA genomes from mot...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
Heteroplasmy-the presence of multiple mitochondrial DNA (mtDNA) haplotypes in an individual-can lead...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
Background: Originally believed to be a rare phenomenon, heteroplasmy - the presence of more than on...
INTRODUCTION Only 2.4% of the 16.5-kb mitochondrial DNA (mtDNA) genome shows homoplasmic variation a...
Distinguishing between maternal relatives through mitochondrial (mt) DNA sequence analysis has been ...
A genetic bottleneck explains the marked changes in mitochondria! DNA (mtDNA) heteroplasmy that are ...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
Common genetic variants of mitochondrial DNA (mtDNA) increase the risk of developing several of the ...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...
Although previous studies have documented a bottleneck in the transmission of mtDNA genomes from mot...
Although previous studies have documented a bottleneck in the transmission of mtDNA genomes from mot...
Although previous studies have documented a bottleneck in the transmission of mtDNA genomes from mot...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
Heteroplasmy-the presence of multiple mitochondrial DNA (mtDNA) haplotypes in an individual-can lead...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
Background: Originally believed to be a rare phenomenon, heteroplasmy - the presence of more than on...
INTRODUCTION Only 2.4% of the 16.5-kb mitochondrial DNA (mtDNA) genome shows homoplasmic variation a...
Distinguishing between maternal relatives through mitochondrial (mt) DNA sequence analysis has been ...
A genetic bottleneck explains the marked changes in mitochondria! DNA (mtDNA) heteroplasmy that are ...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
Common genetic variants of mitochondrial DNA (mtDNA) increase the risk of developing several of the ...
SummaryWe have examined oocytes from a patient with Kearn-Sayre syndrome caused by mtDNA rearrangeme...