Reversal of a mitochondrial DNA defect in human skeletal muscle

[1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J]. NATURE, 1981, 290 (5806) : 457 - 465

[2] ARGOV Z, 1994, DISORDERS VOLUNTARY, P989

[3] BENOIT PW, 1970, J ANAT, V107, P547

[4] ISOLATION AND CHARACTERIZATION OF HUMAN-MUSCLE CELLS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09): : 5623 - 5627

[5] BOULET L, 1992, AM J HUM GENET, V51, P1187

[6] CARLSON BM, 1992, OPHTHALMOLOGY, V99, P582

[7] MELAS MUTATION IN MTDNA BINDING-SITE FOR TRANSCRIPTION TERMINATION FACTOR CAUSES DEFECTS IN PROTEIN-SYNTHESIS AND IN RESPIRATION BUT NO CHANGE IN LEVELS OF UPSTREAM AND DOWNSTREAM MATURE TRANSCRIPTS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) : 4221 - 4225

[8] MITOCHONDRIAL ENCEPHALOMYOPATHIES [J]. ARCHIVES OF NEUROLOGY, 1993, 50 (11) : 1197 - 1208

[9] A novel heteroplasmic tRNA(leu(CUN)) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (11) : 1835 - 1840

[10] GRAEGIORE M, 1984, EUR J BIOCHEM, V142, P49

[1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J]. NATURE, 1981, 290 (5806) : 457 - 465

[2] ARGOV Z, 1994, DISORDERS VOLUNTARY, P989

[3] BENOIT PW, 1970, J ANAT, V107, P547

[4] ISOLATION AND CHARACTERIZATION OF HUMAN-MUSCLE CELLS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09): : 5623 - 5627

[5] BOULET L, 1992, AM J HUM GENET, V51, P1187

[6] CARLSON BM, 1992, OPHTHALMOLOGY, V99, P582

[7] MELAS MUTATION IN MTDNA BINDING-SITE FOR TRANSCRIPTION TERMINATION FACTOR CAUSES DEFECTS IN PROTEIN-SYNTHESIS AND IN RESPIRATION BUT NO CHANGE IN LEVELS OF UPSTREAM AND DOWNSTREAM MATURE TRANSCRIPTS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) : 4221 - 4225

[8] MITOCHONDRIAL ENCEPHALOMYOPATHIES [J]. ARCHIVES OF NEUROLOGY, 1993, 50 (11) : 1197 - 1208

[9] A novel heteroplasmic tRNA(leu(CUN)) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (11) : 1835 - 1840

[10] GRAEGIORE M, 1984, EUR J BIOCHEM, V142, P49