Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations

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  • en
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  • Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations
P60049

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Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations

description
  • Yhteenveto-osa julkaistu myös verkkoaineistona ISBN 978-952-62-0294-5 (PDF)
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name
  • Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations

Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations

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  • Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations
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Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations

datePublished
  • 2013
description
  • Artikkeliväitöskirjan yhteenveto-osa ja 4 eripainosta.
  • kuvitettu
identifier
  • propertyID: FI-MELINDA value: 006533158
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  • 9789526202938
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name
  • Mitochondrial DNA sequence variation in Finnish patients with maternally inherited type 2 diabetes, epilepsy and mitochondrial disease : risk and novel mutations
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  • 112, [61] sivu
P60048
P60050
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  • location: Oulu organizer: Oulun yliopisto
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