Petri Luoma

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

Petri Luoma, Atle Melberg, Juha O. Rinne et al. · The Lancet · 2004 · 540 citations

Neurodegenerative Diseases, Molecular Genetic Study, Genetic Disorder +12

Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin

Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen et al. · The American Journal of Human Genetics · 2005 · 305 citations · Full text

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +10

<i>POLG</i> mutations in neurodegenerative disorders with ataxia but no muscle involvement

G. Van Goethem, Petri Luoma, Maria Rantamäki et al. · Neurology · 2004 · 258 citations

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease

Petri Luoma, Johanna Eerola, Sofia Ahola et al. · Neurology · 2007 · 154 citations

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

Petri Luoma, Ningguang Luo, Wolfgang N. Löscher et al. · Human Molecular Genetics · 2005 · 110 citations