G8363A mutation in the mitochondrial DNA transfer ribonucleic acid Lys gene: another cause of Leigh syndrome. - Shtilbans,A.; Shanske,S.; Goodman,S.; Sue,C.M.; Bruno,C.; Johnson,T.L.; Lava,N.S.; Waheed,N.; DiMauro,S. (J Child Neurol, 2000)