Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.

AN ELECTRON-TRANSPORT SYSTEM ASSOCIATED WITH THE OUTER MEMBRANE OF LIVER MITOCHONDRIA

1967 • 2,311 citations

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1988 • 1,806 citations

Deletions of mitochondrial DNA in Kearns‐Sayre syndrome

1988 • 730 citations

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1989 • 637 citations

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

1990 • 456 citations

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA

1990 • 341 citations

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

1988 • 137 citations

Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens

1978 • 135 citations

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms

1989 • 102 citations

Shuttling of integrated vectors from mammalian cells toE. coli is mediated by head-to-tail multimeric inserts

1985 • 30 citations