Publikationen

Holme, E.; Greter, J.; Jacobson, C. E.; Larsson, N.G.; Lindstedt, S.; Nilsson, K. O.; Oldfors, A.; Tulinius, M.: Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria. Pediatr Res 32 (6), S. 731 - 5 (1992)

Larsson, N.G.; Tulinius, M. H.; Holme, E.; Oldfors, A.; Andersen, O.; Wahlstrom, J.; Aasly, J.: Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. Am J Hum Genet 51 (6), S. 1201 - 12 (1992)

Larsson, N.G.; Holme, E.: Multiple short direct repeats associated with single mtDNA deletions. Biochim Biophys Acta 1139 (4), S. 311 - 4 (1992)

Oldfors, A.; Larsson, N.G.; Holme, E.; Tulinius, M.; Kadenbach, B.; Droste, M.: Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres. J Neurol Sci 110 (1-2), S. 169 - 77 (1992)

Larsson, N.G.; Eiken, H. G.; Boman, H.; Holme, E.; Oldfors, A.; Tulinius, M. H.: Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child. Am J Hum Genet 50 (2), S. 360 - 3 (1992)