Tarja Lamminen

mtDNA Haplotype Analysis in Finnish Families with Leber Hereditary Optic Neuroretinopathy

P. Sistonen, K. Huoponen, M. Savontaus, 1997, European journal of human genetics : EJHG.

Mutations in subunit 6 of the F1F0‐ATP synthase cause two entirely different diseases

M. Wikström, M. Savontaus, A. Majander, 1997, FEBS letters.