File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome

TitleA novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome
Authors
Issue Date2008
PublisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/cca
Citation
Clinica Chimica Acta, 2008, v. 398 n. 1-2, p. 157-158 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148585
ISSN
2015 Impact Factor: 2.799
2015 SCImago Journal Rankings: 1.040
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLam, CWen_US
dc.contributor.authorKong, APSen_US
dc.contributor.authorTsui, TKCen_US
dc.contributor.authorOzaki, Ren_US
dc.contributor.authorChan, HMen_US
dc.contributor.authorTong, SFen_US
dc.contributor.authorSiu, TSen_US
dc.contributor.authorTam, Sen_US
dc.contributor.authorChan, JCNen_US
dc.date.accessioned2012-05-29T06:13:54Z-
dc.date.available2012-05-29T06:13:54Z-
dc.date.issued2008en_US
dc.identifier.citationClinica Chimica Acta, 2008, v. 398 n. 1-2, p. 157-158en_US
dc.identifier.issn0009-8981en_US
dc.identifier.urihttp://hdl.handle.net/10722/148585-
dc.languageengen_US
dc.publisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ccaen_US
dc.relation.ispartofClinica Chimica Actaen_US
dc.subject.meshAdulten_US
dc.subject.meshAgeden_US
dc.subject.meshCreatinine - Blooden_US
dc.subject.meshDna Mutational Analysisen_US
dc.subject.meshDiabetes Mellitus, Type 2 - Geneticsen_US
dc.subject.meshFamilyen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshKidney Diseases - Genetics - Metabolismen_US
dc.subject.meshKidney Function Testsen_US
dc.subject.meshMaleen_US
dc.subject.meshMetabolic Syndrome X - Genetics - Metabolismen_US
dc.subject.meshMutation - Geneticsen_US
dc.subject.meshOrganic Anion Transporters - Geneticsen_US
dc.subject.meshOrganic Cation Transport Proteins - Geneticsen_US
dc.subject.meshUric Acid - Metabolismen_US
dc.titleA novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndromeen_US
dc.typeArticleen_US
dc.identifier.emailLam, CW:ching-wanlam@pathology.hku.hken_US
dc.identifier.authorityLam, CW=rp00260en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/j.cca.2008.08.005en_US
dc.identifier.pmid18760270-
dc.identifier.scopuseid_2-s2.0-54049090314en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-54049090314&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume398en_US
dc.identifier.issue1-2en_US
dc.identifier.spage157en_US
dc.identifier.epage158en_US
dc.identifier.isiWOS:000261074200033-
dc.publisher.placeNetherlandsen_US

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats