D. Alves, M. E. Calmeiro, C. Macário, and R. Silva, Family phenotypic heterogeneity caused by mitochondrial DNA mutation A3243G, Acta Med Port, vol.30, pp.581-586, 2017.

J. Finsterer, M. Frank, and A. Mishra, Genetic background and phenotypic Revista Científica da Ordem dos Médicos www

, Acta Med Port, vol.30, issue.9, pp.664-666, 2017.

, heterogeneity of MELAS and maternally inherited diabetes and deafness, Int J Clin Exp Pathol, vol.8, pp.15439-15480, 2015.

J. Finsterer and P. S. Bindu, Therapeutic strategies for mitochondrial disorders, Pediatr Neurol, vol.52, pp.302-315, 2015.

. Josef-finsterer?-1 and Z. Sinda,

K. Rudolfstiftung,

, Autor correspondente: Josef Finsterer. fifigs1@yahoo.de Recebido: 22 de setembro de 2017 -Aceite: 25 de setembro de 2017 | Copyright © Ordem dos Médicos, 2017.