mtDNA is transmitted through the maternal line and its sequence variability, which is population specific, is assumed to be phenotypically neutral. However, several studies have shown associations between the variants defining some genetic backgrounds and the susceptibility to several pathogenic phenotypes, including neurodegenerative diseases. Many of these studies have found that some of these variants impact many of these phenotypes, including the ones defining the Caucasian haplogroups H, J, and Uk, while others, such as the ones defining the T haplogroup, have phenotype specific associations. In this review, we will focus on those that have shown a pleiotropic effect in population studies in neurological diseases. We will also explore ...
SummaryMitochondrial diseases cause a range of clinical manifestations even in patients carrying the...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Distinct clinical syndromes have been associated with pathogenic MT-ATP6 variants. In this cohort st...
mtDNA is transmitted through the maternal line and its sequence variability, which is population spe...
Mitochondrial DNA mutations are an important cause of neurological disease. The clinical presentatio...
AbstractMitochondrial DNA mutations are an important cause of neurological disease. The clinical pre...
AbstractMitochondria are essential organelles within the cell where most of the energy production oc...
AbstractThis study examines the relationship of genotype to phenotype in 14 unselected patients who ...
A rapidly expanding catalog of neurogenetic disorders has encouraged a diagnostic shift towards earl...
Abstract: Mitochondrial diseases are highly heterogeneous metabolic disorders caused by genetic alte...
PhD ThesisMitochondria are dynamic organelles whose principal role is the generation of cellular ene...
[Background] Mitochondrial DNA (mtDNA) encodes 37 genes necessary for synthesizing 13 essential subu...
Mitochondrial diseases (MDs) are a large group of genetically determined multisystem disorders, char...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Mitochondrial DNA mutations cause disease in > 1 in 5000 of the population, and similar to 1 in 2...
SummaryMitochondrial diseases cause a range of clinical manifestations even in patients carrying the...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Distinct clinical syndromes have been associated with pathogenic MT-ATP6 variants. In this cohort st...
mtDNA is transmitted through the maternal line and its sequence variability, which is population spe...
Mitochondrial DNA mutations are an important cause of neurological disease. The clinical presentatio...
AbstractMitochondrial DNA mutations are an important cause of neurological disease. The clinical pre...
AbstractMitochondria are essential organelles within the cell where most of the energy production oc...
AbstractThis study examines the relationship of genotype to phenotype in 14 unselected patients who ...
A rapidly expanding catalog of neurogenetic disorders has encouraged a diagnostic shift towards earl...
Abstract: Mitochondrial diseases are highly heterogeneous metabolic disorders caused by genetic alte...
PhD ThesisMitochondria are dynamic organelles whose principal role is the generation of cellular ene...
[Background] Mitochondrial DNA (mtDNA) encodes 37 genes necessary for synthesizing 13 essential subu...
Mitochondrial diseases (MDs) are a large group of genetically determined multisystem disorders, char...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Mitochondrial DNA mutations cause disease in > 1 in 5000 of the population, and similar to 1 in 2...
SummaryMitochondrial diseases cause a range of clinical manifestations even in patients carrying the...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Distinct clinical syndromes have been associated with pathogenic MT-ATP6 variants. In this cohort st...