Carlos T. Moraes

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

S. Dimauro, E. Schon, R. Rizzuto, 1990, Nucleic acids research.

Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region

S. Dimauro, E. Schon, C. Moraes, 1991, Molecular and cellular biology.

Mitochondrial DNA depletion

S. Dimauro, M. Mancuso, A. Marina, 2002, Neurology.

Widespread tissue distribution of mitochondrial DNA deletions in Kearns‐Sayre syndrome

S. Dimauro, C. Moraes, A. Lombès, 1990, Neurology.

Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?

S. Dimauro, E. Schon, M. Zeviani, 1991, American journal of medical genetics.

A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene

S. Dimauro, E. Schon, C. Moraes, 1995, Neuromuscular Disorders.