Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome

Article

Abstract: Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a multi

Palabras claves:

Heteroplasmy, MELAS syndrome, Mitochondrial haplogroup, MT-TL1 gene, MtDNA, Venezuelan patients

Autores:

Casique L., Domínguez C.L., Florez I., M. De Lucca, Mahfoud A., Pirrone I., Ramirez J.L., Rodríguez D., Rodríguez T.

Fuentes:

scopus