F. M. Santorelli

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.

S. Dimauro, F. Santorelli, C. Casali, 1999, American journal of human genetics.

Mutation analysis in 16 patients with mtDNA depletion

E. Bertini, R. Carrozzo, N. Petit, 2003, Human mutation.

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

S. Dimauro, F. Santorelli, L. Vilarinho, 1997, Biochemical and biophysical research communications.

Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy.

F. Santorelli, S. Petrillo, A. Romano, 2015, Human molecular genetics.

A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy.

S. Dimauro, F. Santorelli, D. González-Halphen, 1995, Biochemical and biophysical research communications.