… Here, we review all the mitochondrial carrier-related diseases known until now, … review
focusses on the subgroup of mitochondrial diseases that are caused by mutations in the genes …

… transporters of the SLC25 family have been well characterized biochemically and …
disorders caused by mutations in the SLC25 nuclear genes that encode mitochondrial carriers, a …

… Only recently numerous diseases resulting from mutations in nuclear genes encoding … (particularly
in view of the fact that the function of about 20 human genes of the SLC25 family has …

… In this review, after illustrating typical MCF structural and functional … the order of the SLC25
gene numbers. The names of the … Mutations in the gene SLC25A13 coding isoform 2 of the …

… mutations in the SLC25 genes have been shown to be responsible for 11 diseases, highlighting
the important role of SLC25 … reader is referred to the review published in the first special …

… review to cover the current knowledge on the role of SLC25 … also implicated mutations in
the SLC25a7 gene as a cause of … human genes by Palmieri's group revealed an SLC25 family …

… SLC25A11 is considered a tumor suppressor gene in metastatic paragangliomas and
pheochromocytomas, with mutations linked to an increased risk of metastatic disease. …

… The objective of this review is to summarize the current … , mutations of nuclear genes
involved in mitochondrial DNA (… levels as well as the diseases associated with its dysfunction. …

… This review suggests that the SLC25 family could be used for … Mutations of almost every
mtDNA-encoded gene have been … of polymorphic SLC25 genes in certain disorders [20]. Future …

… Mitochondrial carriers (MCs) are a superfamily of transporters named the MCF, or in mammals
SLC25 (solute … Recently, a genetic disease (OMIM 616794 ) caused by mutations in the …