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Luoma PT

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Missing references?

Publications:

Title Authors Year Journal
Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease. Luoma PT 2007 Neurology
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome. Luoma PT 2005 Human molecular genetics
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin. Luoma PT 2005 American journal of human genetics

Version:20241007

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