lnu.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden - a genealogical study
University of Kalmar, School of Human Sciences.
Show others and affiliations
1995 (English)In: Journal of Medical Genetics, Vol. 32, p. 344-347Article in journal (Refereed) Published
Place, publisher, year, edition, pages
1995. Vol. 32, p. 344-347
Research subject
Social Sciences, Sociology
Identifiers
URN: urn:nbn:se:lnu:diva-1424OAI: oai:DiVA.org:lnu-1424DiVA, id: diva2:308296
Available from: 2010-04-06 Created: 2010-04-06 Last updated: 2011-09-16Bibliographically approved

Open Access in DiVA

No full text in DiVA

Authority records BETA

Drugge, Ulf

Search in DiVA

By author/editor
Drugge, Ulf
By organisation
School of Human Sciences

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 36 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf