We sequenced all genes of mitochondrial tRNAs of a patient with chronic progressive external ophthalmoplegia with 5% ragged red fibres and 15% COX-negative fibres but without macrorearrangements of mitochondrial DNA (mtDNA). Direct sequencing showed a novel heteroplasmic G>A substitution in position 12316 of tRNA(Leu(CUN)) gene. This change destroys a highly conserved G-C base coupling in tRNA TpsiC branch. By RFLP analysis we could demonstrate different degrees of heteroplasmy in different patient's tissues. This alteration, absent in a population of 110 patients with different encephalomyopathies, can be considered pathogenic: it is the tenth tRNA(Leu(CUN)) pathogenic mutation described up to date
Chronic progressive external ophthalmoplegia is a mitochondrial disorder usually caused by single or...
We identified a double mutation in a patient with chronic progressive external ophthalmoplegia, loca...
We have investigated nine children with infantile onset of mitochondrial myopathy and two adults wit...
We sequenced all genes of mitochondrial tRNAs of a patient with chronic progressive external ophthal...
We have sequenced all mitochondrial tRNA genes from a patient with chronic progressive external opht...
We sequenced all mitochondrial tRNA genes from a patient with sporadic external ophthalmoplegia (PEO...
We have sequenced the entire mitochondrial DNA (mtDNA) from a 54-year-old man with chronic progressi...
We describe a new mutation in the tRNA(Ala) gene, a T-->C transition at nucleotide position 5628, in...
Chronic progressive external ophthalmoplegia (CPEO) is caused by a decreased oxidative phosphorylati...
We report a sporadic case of chronic progressive external ophthalmoplegia associated with ragged red...
We describe a new mutation in the tRNAAla gene, a T→C transition at nucleotide position 5628, in a 6...
Mutations in mitochondrially encoded tRNA genes have been described in a variety of neurological dis...
We describe a patient who suffered from impaired ocular motility from age 10 years and at 16 years d...
Mitochondrial disorders are often associated with mutations in mitochondrial tRNA. Independent obser...
A 21-year-old woman described proximal muscle weakness since early childhood. At age 16, she develop...
Chronic progressive external ophthalmoplegia is a mitochondrial disorder usually caused by single or...
We identified a double mutation in a patient with chronic progressive external ophthalmoplegia, loca...
We have investigated nine children with infantile onset of mitochondrial myopathy and two adults wit...
We sequenced all genes of mitochondrial tRNAs of a patient with chronic progressive external ophthal...
We have sequenced all mitochondrial tRNA genes from a patient with chronic progressive external opht...
We sequenced all mitochondrial tRNA genes from a patient with sporadic external ophthalmoplegia (PEO...
We have sequenced the entire mitochondrial DNA (mtDNA) from a 54-year-old man with chronic progressi...
We describe a new mutation in the tRNA(Ala) gene, a T-->C transition at nucleotide position 5628, in...
Chronic progressive external ophthalmoplegia (CPEO) is caused by a decreased oxidative phosphorylati...
We report a sporadic case of chronic progressive external ophthalmoplegia associated with ragged red...
We describe a new mutation in the tRNAAla gene, a T→C transition at nucleotide position 5628, in a 6...
Mutations in mitochondrially encoded tRNA genes have been described in a variety of neurological dis...
We describe a patient who suffered from impaired ocular motility from age 10 years and at 16 years d...
Mitochondrial disorders are often associated with mutations in mitochondrial tRNA. Independent obser...
A 21-year-old woman described proximal muscle weakness since early childhood. At age 16, she develop...
Chronic progressive external ophthalmoplegia is a mitochondrial disorder usually caused by single or...
We identified a double mutation in a patient with chronic progressive external ophthalmoplegia, loca...
We have investigated nine children with infantile onset of mitochondrial myopathy and two adults wit...