Significados de mitochondrial dna depletion syndrome em inglês

The diagnosis is infantile onset encephalomyopathic mitochondrial DNA depletion syndrome, referred to generally as MDDS.

Charlie has encephalomyopathic mitochondrial DNA depletion syndrome.

Severe TK2 deficiency is associated with early-onset fatal mitochondrial DNA depletion syndrome, while less severe deficiencies result in late-onset phenotypes.

Mutations in FBXL4 (F-Box and Leucine rich repeat protein 4), a nuclear-encoded mitochondrial protein with an unknown function, cause mitochondrial DNA depletion syndrome.