J. Kaukonen

Localization of the APECED protein in distinct nuclear structures.

L. Peltonen, M. Pelto-huikko, I. Ulmanen, 1999, Human molecular genetics.

An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.

L. Peltonen, J. Weissenbach, G. Comi, 1996, American journal of human genetics.

IMPDH2: a new gene associated with dominant juvenile-onset dystonia-tremor disorder

T. Torkkeli, V. Velagapudi, J. C. Landoni, 2021, European Journal of Human Genetics.

Role of adenine nucleotide translocator 1 in mtDNA maintenance.

L. Peltonen, G. Comi, V. Tiranti, 2000, Science.

An autosomal locus predisposing to deletions of mitochondrial DNA

L. Peltonen, J. Weissenbach, M. Zeviani, 1995, Nature Genetics.

Diseases caused by nuclear genes affecting mtDNA stability.

A. Suomalainen, J. Kaukonen, 2001, American journal of medical genetics.

Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study

L. Peltonen, J. Rinne, K. Majamaa, 2004, The Lancet.

A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia.

L. Peltonen, G. Comi, M. Zeviani, 1999, American journal of human genetics.