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Citation: Saviranta, Petri et al., Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq, American journal of human genetics , 42(1), 1988, pp. 84-88

Authors: Nikoskelainen, Eeva K. Savontaus, Marja-Liisa Vilkki, Johanna

Citation: K. Nikoskelainen, Eeva et al., Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy, American journal of human genetics , 47-I(1), 1990, pp. 95-100

Authors: Vilkki, Johanna Savontaus, Marja-Liisa Nikoskelainen, Eeva K.

Citation: Vilkki, Johanna et al., Genetic heterogeneity in leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism, American journal of human genetics , 45-I(2), 1989, pp. 206-211

Authors: Hudson, Gavin Carelli, Valerio Spruijt, Liesbeth Gerards, Mike Mowbray, Catherine Achilli, Alessandro Pyle, Angela Elson, Joanna Howell, Neil La Morgia, Chiara Valentino, Maria Lucia Huoponen, Kirsi Savontaus, Marja-Liisa Nikoskelainen, Eeva Sadun, Alfredo A. Salomao, Solange R. Belfort Jr., Rubens Griffiths, Philip Yu-Wai-Man, Patrick De Coo, Rene F.M. Chinnery, Patrick F.

Citation: Hudson, Gavin et al., Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA.Haplogroup Background, American journal of human genetics , 81(2), 2007, pp. 228-233

Authors: Huoponen, Kirsi Vilkki, Johanna Aula, Pertti Nikoskelainen, Eeva K. Savontaus, Marja-Liisa

Citation: Huoponen, Kirsi et al., A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy., American journal of human genetics , 48-II(6), 1991, pp. 1147-1153