Cadasil : molecular studies on the most common hereditary vascular dementing disorder

URI: http://urn.fi/URN:NBN:fi:bib:me:W00561389500
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  • Cadasil : molecular studies on the most common hereditary vascular dementing disorder
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Cadasil : molecular studies on the most common hereditary vascular dementing disorder

URI: http://urn.fi/URN:NBN:fi:bib:me:I00565373701
description
  • Myös painettuna ISBN 978-952-92-5519-1
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  • Cadasil : molecular studies on the most common hereditary vascular dementing disorder

Cadasil : molecular studies on the most common hereditary vascular dementing disorder

URI: http://urn.fi/URN:NBN:fi:bib:me:I00561389501
description
  • Myös verkkoaineistona ISBN 978-952-92-5516-4 (PDF)
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  • Cadasil : molecular studies on the most common hereditary vascular dementing disorder
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Cadasil : molecular studies on the most common hereditary vascular dementing disorder

URI: http://urn.fi/URN:NBN:fi:bib:me:I00565373700
bookFormat
datePublished
  • 2009
description
  • Artikkeliväitöskirjan yhteenveto-osa.
  • Nimeke PDF-nimiösivulta.
identifier
  • propertyID: FI-FENNI value: 916876
  • propertyID: FI-MELINDA value: 005653737
  • propertyID: skl value: fx916876
isbn
  • 9789521055164
isPartOf
name
  • Cadasil : molecular studies on the most common hereditary vascular dementing disorder
numberOfPages
  • 1 PDF-tiedosto (84 s.)
P60048
P60050
publication
  • location: Helsinki organizer: Helsingin yliopisto
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Cadasil : molecular studies on the most common hereditary vascular dementing disorder

URI: http://urn.fi/URN:NBN:fi:bib:me:I00561389500
datePublished
  • 2009
description
  • Artikkeliväitöskirjan yhteenveto-osa ja 4 eripainosta.
  • kuvitettu
  • Nimiösivulla myös: Haartman Institute, Department of Pathology and Institute of Biomedecine, Protein Chemistry Unit, Faculty of Medicine & Department of Biological and Environmental Sciences, Faculty of Biosciences
identifier
  • propertyID: FI-FENNI value: 916874
  • propertyID: FI-MELINDA value: 005613895
  • propertyID: skl value: fx916874
isbn
  • 9789529255191
isPartOf
name
  • Cadasil : molecular studies on the most common hereditary vascular dementing disorder
numberOfPages
  • 84, [65] sivu
P60048
P60050
publication
  • location: Helsinki organizer: Saara Tikka
publisher
  • Saara Tikka

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