Concepedia

M L Savontaus

ML

16

Publications

2.7K

Citations

16

H-Index

1987

Active since

Affiliations

University of Turku(Current)

University of Helsinki

Institute for Molecular Medicine Finland

Umeå University

Karolinska University Hospital

M L Savontaus is an author at University of Turku specializing in genetics, medicine, and neuropathology.

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Publications per year

1987–2008

16

Publications

16

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Alan H. Beggs, Mary B. Moyer, S. Scherpf et al. · PubMed · 1989 · 961 citations

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.

Kirsi Huoponen, Johanna Vilkki, P Aula et al. · PubMed · 1991 · 393 citations

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

Eeva Nikoskelainen, R. J. Marttila, Kirsi Huoponen et al. · Journal of Neurology Neurosurgery & Psychiatry · 1995 · 265 citations · Full text

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Anu Suomalainen, Anna Majander, Matti Haltia et al. · Journal of Clinical Investigation · 1992 · 242 citations · Full text

, , +15

Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

Anna Majander, Kirsi Huoponen, M L Savontaus et al. · FEBS Letters · 1991 · 166 citations · Full text

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