mtDNA in congenital myotonic dystrophy.

Por Thyagarajan, D, Byrne, E, Noer, A S, Lertrit, P, Kapsa, R, Marzuki, S
Publicado em 1993

A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.

Por Noer, A S, Sudoyo, H, Lertrit, P, Thyagarajan, D, Utthanaphol, P, Kapsa, R, Byrne, E, Marzuki, S
Publicado em 1991

mtDNA replicative potential remains constant during ageing: polymerase gamma activity does not correlate with age related cytochrome oxidase activity decline in platelets.

Por Kapsa, R M, Quigley, A F, Han, T F, Jean-Francois, M J, Vaughan, P, Byrne, E
Publicado em 1998

A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.

Por Lertrit, P, Noer, A S, Jean-Francois, M J, Kapsa, R, Dennett, X, Thyagarajan, D, Lethlean, K, Byrne, E, Marzuki, S
Publicado em 1992