Welcome to Suomalainen-Wartiovaara group pages

The mission of Wartiovaara lab is to understand the molecular background of mitochondrial disorders, and use that knowledge to develop diagnosis and therapy. Mitochondrial dysfunction has shown out to be a common cause of human inherited disease, with amazing clinical variability, from neonatal fatal multisystem disorders to diabetes, neurodegeneration, dysfertility or tumorigenesis of adult age.
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