Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Biochemical defects in familial hypercholesterolemia]

T P Leren, H Tolleshaug

    Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
    |November 20, 1987
    PubMed
    Summary

    No abstract available in PubMed .

    Related Experiment Videos

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia.

    Nutrition, metabolism, and cardiovascular diseases : NMCD·2017
    Same author

    Genetics of hypertrophic cardiomyopathy in Norway.

    Clinical genetics·2013
    Same author

    Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases.

    International journal of legal medicine·2012
    Same author

    Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy.

    Forensic science international·2011
    Same author

    The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasis.

    Journal of internal medicine·2009
    Same author

    Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.

    Scandinavian journal of clinical and laboratory investigation·2008