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
Saved in:
| Genre | |
|---|---|
| Physical Description |
77, [29] sivua : kuvitettu ; 25 cm Julkaistu myös verkkoaineistona |
| Language |
English |
| Language of Original Work |
English |
| Item Description |
Artikkeliväitöskirjan yhteenveto-osa ja 3 eripainosta. 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. |
| Published |
Helsinki :
University of Helsinki,
2015
|
| Dissertation Note | Väitöskirja : Helsingin yliopisto, 2015 |
| Classification | |
| Subjects | |
| Manufacturer | (Helsinki : Unigrafia) |
| Additional Information | Padmini P. Polinati |
| Verkkoaineisto (PDF) |
978-951-51-1545-4 |
| ISBN |
978-951-51-1544-7 nidottu |
| Get full text | |