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Works by Kervinen, Marko

Results: 4

1

The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 17, p. 2543, doi. 10.1093/hmg/ddl176

By:

Kervinen, Marko;
Hinttala, Reetta;
Helander, Heli M.;
Kurki, Sari;
Uusimaa, Johanna;
Finel, Moshe;
Majamaa, Kari;
Hassinen, Ilmo E.

Publication type:

Article

2

Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms.

Published in:

Acta Ophthalmologica (1755375X), 2016, v. 94, n. 1, p. 83, doi. 10.1111/aos.12897

By:

Widgren, Paula;
Hurme, Anri;
Falck, Aura;
Keski ‐ Filppula, Riikka;
Remes, Anne M;
Moilanen, Jukka;
Majamaa, Kari;
Kervinen, Marko;
Uusimaa, Johanna

Publication type:

Article

3

Leber hereditary optic neuropathy mutations and toxic-genetic optic neuropathy - Authors' response.

Published in:

Acta Ophthalmologica (1755375X), 2014, v. 92, n. 1, p. e78, doi. 10.1111/aos.12089

By:

Kervinen, Marko;
Widgren, Paula;
Saarela, Ville;
Uusimaa, Johanna;
Remes, Anne

Publication type:

Article

4

Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.

Published in:

Acta Ophthalmologica (1755375X), 2013, v. 91, n. 7, p. 630, doi. 10.1111/j.1755-3768.2012.02506.x

By:

Korkiamäki, Paula;
Kervinen, Marko;
Karjalainen, Karoliina;
Majamaa, Kari;
Uusimaa, Johanna;
Remes, Anne M.

Publication type:

Article