A study on genetic mutations involving mitochondrial disorders :

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  • en
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name
  • 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
P60049

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A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis

description
  • Julkaistu myös verkkoaineistona
isPartOf
name
  • 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 :

isbn
  • 9789515115454
isPartOf
name
  • 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

datePublished
  • 2015
description
  • 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.
identifier
  • propertyID: FI-MELINDA value: 007703902
isbn
  • 9789515115447
isPartOf
name
  • A study on genetic mutations involving mitochondrial disorders : a diagnostic approach and application of human iPSCs to understand disease pathogenesis
numberOfPages
  • 77, [29] s.
P60048
P60050
publication
  • location: Helsinki organizer: Helsingin yliopisto
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