Heidi K. Soini

Homozygous W748S mutation in the <i>POLG1</i> gene in patients with juvenile‐onset Alpers syndrome and status epilepticus

Johanna Uusimaa, Reetta Hinttala, Heikki Rantala et al. · Epilepsia · 2008 · 79 citations · Full text

Adult‐onset ataxia and polyneuropathy caused by mitochondrial 8993T→C mutation

Maria Rantamäki, Heidi K. Soini, Saara Finnilä et al. · Annals of Neurology · 2005 · 39 citations

Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene

Anne M. Remes, Reetta Hinttala, Mikko Kärppä et al. · Parkinsonism & Related Disorders · 2008 · 37 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus

Heidi K. Soini, Jukka S. Moilanen, Saara Finnilä et al. · BMC Research Notes · 2012 · 25 citations · Full text

Novel non‐neutral mitochondrial <scp>DNA</scp> mutations found in childhood acute lymphoblastic leukemia

Tekla Järviaho, Anri Hurme‐Niiranen, Heidi K. Soini et al. · Clinical Genetics · 2017 · 24 citations