Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death

Sequence and organization of the human mitochondrial genome

1981 • 9,348 citations

Cytochrome c oxidase deficiency in leigh syndrome

1987 • 368 citations

Mitochondrial Encephalomyopathies

1993 • 297 citations

The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome

1993 • 259 citations

Respiratory Arrest in Infants Secondary to Gastroesophageal Reflux

1977 • 185 citations

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles.

1994 • 181 citations

SUDDEN AND UNEXPECTED DEATH IN INFANCY: A REVIEW OF THE WORLD LITERATURE 1954-1966

1967 • 158 citations

Esophageal reflux—an unrecognized cause of recurrent obstructive bronchitis in children

1976 • 132 citations

Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.

1994 • 127 citations

Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases

1991 • 93 citations

The risk of sudden infant death from gastroesophageal reflux

1991 • 78 citations

Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA<sup>(UUR)</sup> gene

1993 • 72 citations

Complementation of Mutant and Wild-Type Human Mitochondrial DNAs Coexisting Since the Mutation Event and Lack of Complementation of DNAs Introduced Separately into a Cell within Distinct Organelles

1994 • 67 citations

Sudden Infant Death Syndrome and Inherited Disorders of Fatty Acid β-Oxidation

1990 • 50 citations

MELAS point mutation with unusual clinical presentation

1993 • 34 citations

Inherited metabolic diseases in the sudden infant death syndrome.

1991 • 33 citations