A study on genetic mutations involving mitochondrial disorders :
A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis
A study on genetic mutations involving mitochondrial disorders :
A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis
A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis
A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis
Artikkeliväitöskirjan yhteenveto-osa ja 3 eripainosta.
kuvitettu
Nimiösivulla myös: Faculty of Medicine - Doctoral School in Health Sciences, Doctoral Programme in Clinical Research & Institute of Biomedicine, Department of Clinical Molecular Medicine, Research Program Unit, Molecular Neurology, University of Helsinki.
A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis