A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.

由 Huoponen, K, Vilkki, J, Aula, P, Nikoskelainen, E K, Savontaus, M L
出版 1991

Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.

由 Brown, M. D., Torroni, A., Huoponen, K., Chen, Y. S., Lott, M. T., Wallace, D. C.
出版 1994

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

由 Nikoskelainen, E K, Marttila, R J, Huoponen, K, Juvonen, V, Lamminen, T, Sonninen, P, Savontaus, M L
出版 1995

Classification of European Mtdnas from an Analysis of Three European Populations

由 Torroni, A., Huoponen, K., Francalacci, P., Petrozzi, M., Morelli, L., Scozzari, R., Obinu, D., Savontaus, M. L., Wallace, D. C.
出版 1996