M. Lehtonen

Technical knockout, a Drosophila model of mitochondrial deafness.

J. Toivonen, K. O’Dell, N. Petit, 2001, Genetics.

Phylogenetic network for European mtDNA.

M. Lehtonen, S. Finnilä, K. Majamaa, 2001, American journal of human genetics.

Association of angiotensin converting enzyme and plasminogen activator inhibitor-1 promoter gene polymorphisms with features of the insulin resistance syndrome in patients with premature coronary heart disease.

M. Laakso, M. Lehtonen, S. Lehto, 2001, Atherosclerosis.

Mitochondrial DNA sequence variation in patients with sensorineural hearing impairment and in the Finnish population

M. Lehtonen, 2002 .

Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment

M. Lehtonen, K. Majamaa, I. Hassinen, 2000, European Journal of Human Genetics.

Increased variation in mtDNA in patients with familial sensorineural hearing impairment

M. Lehtonen, K. Majamaa, J. Moilanen, 2003, Human Genetics.