J. Zhang, J. Guo, W. Fang, Q. Jun, and K. Shi, Clinical features of MELAS and its relation with A3243G gene point mutation, Int J Clin Exp Pathol, vol.8, pp.13411-13416, 2015.

J. Mayr, A. Moslemi, H. Förster, A. Kamper, C. Idriceanu et al., A novel sporadic mutation G14739A of the mitochondrial tRNAGlu in a girl with exercise intolerance, Neuromuscular Disorders, vol.16, issue.12, pp.874-881, 2006.
DOI : 10.1016/j.nmd.2006.08.010

R. Mcfarland, R. Taylor, and D. Turnbull, A neurological perspective on mitochondrial disease, The Lancet Neurology, vol.9, issue.8, pp.829-869, 2010.
DOI : 10.1016/S1474-4422(10)70116-2

J. Lin, C. Zhao, J. Lu, H. Wang, W. Zhu et al., associated with MELAS, Mitochondrial DNA, vol.101, issue.1, pp.56-62, 2014.
DOI : 10.1371/journal.pone.0027750

Y. Hsu, H. Yogasundaram, N. Parajuli, L. Valtuille, C. Sergi et al., MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesis, Heart Failure Reviews, vol.12, issue.Pt 2, pp.103-119, 2015.
DOI : 10.1007/s10741-015-9524-5

S. Reato, S. Spartà, D. Este, and D. , Intraventricular conduction disturbances and paroxysmal atrioventricular block in a young patient with MELAS, Journal of Cardiovascular Medicine, vol.16, issue.2, pp.100-103, 2015.
DOI : 10.2459/JCM.0b013e3283410351

J. Finsterer, Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation, Acta Neurologica Scandinavica, vol.20, issue.2, pp.1-14, 2007.
DOI : 10.1007/s00401-003-0716-z

C. Steriade, D. Andrade, H. Faghfoury, M. Tarnopolsky, and P. Tai, Mitochondrial Encephalopathy With Lactic Acidosis and Stroke-like Episodes (MELAS) May Respond to Adjunctive Ketogenic Diet, Pediatric Neurology, vol.50, issue.5, pp.498-502, 2014.
DOI : 10.1016/j.pediatrneurol.2014.01.009