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

A microradiochemical assay for urate oxidase

T B Friedman, C R Merrill

    Analytical Biochemistry
    |September 1, 1973
    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

    Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

    Clinical genetics·2016
    Same author

    Unresolved questions regarding human hereditary deafness.

    Oral diseases·2016
    Same author

    DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3.

    Clinical genetics·2012
    Same author

    DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

    Clinical genetics·2009
    Same author

    Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.

    Clinical genetics·2009
    Same author

    USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

    Clinical genetics·2008