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Suomalainen A

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Title Authors Year Journal
Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study. Suomalainen A Lancet
Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol {gamma} Suomalainen A 2011 Nucleic acids research
Functional analysis of H. sapiens DNA polymerase gamma spacer mutation W748S with and without common variant E1143G. Suomalainen A 2010 Biochimica et biophysica acta
Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease. Suomalainen A 2007 Neurology
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Suomalainen A 2006 Brain : a journal of neurology
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome. Suomalainen A 2005 Human molecular genetics
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin. Suomalainen A 2005 American journal of human genetics
Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence? Suomalainen A 2005 Acta neuropathologica
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA. Suomalainen A 2004 Nucleic acids research
POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. Suomalainen A 2004 Neurology

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