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Article: DNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese population

TitleDNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese population
Authors
Issue Date2009
PublisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/cca
Citation
Clinica Chimica Acta, 2009, v. 400 n. 1-2, p. 132-134 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148594
ISSN
2023 Impact Factor: 3.2
2023 SCImago Journal Rankings: 1.016
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLau, KCen_US
dc.contributor.authorLam, CWen_US
dc.contributor.authorFong, Ben_US
dc.contributor.authorSiu, TSen_US
dc.contributor.authorTam, Sen_US
dc.date.accessioned2012-05-29T06:13:58Z-
dc.date.available2012-05-29T06:13:58Z-
dc.date.issued2009en_US
dc.identifier.citationClinica Chimica Acta, 2009, v. 400 n. 1-2, p. 132-134en_US
dc.identifier.issn0009-8981en_US
dc.identifier.urihttp://hdl.handle.net/10722/148594-
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.meshAsian Continental Ancestry Group - Geneticsen_US
dc.subject.meshChilden_US
dc.subject.meshChinaen_US
dc.subject.meshDna - Geneticsen_US
dc.subject.meshFamilyen_US
dc.subject.meshFemaleen_US
dc.subject.meshFerrochelatase - Geneticsen_US
dc.subject.meshGene Expression Regulationen_US
dc.subject.meshGene Frequencyen_US
dc.subject.meshGenotypeen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMutationen_US
dc.subject.meshPedigreeen_US
dc.subject.meshPolymorphism, Geneticen_US
dc.subject.meshProtoporphyria, Erythropoietic - Diagnosis - Geneticsen_US
dc.subject.meshYoung Adulten_US
dc.titleDNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese populationen_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.2008.09.031en_US
dc.identifier.pmid18976643en_US
dc.identifier.scopuseid_2-s2.0-57949106639en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-57949106639&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume400en_US
dc.identifier.issue1-2en_US
dc.identifier.spage132en_US
dc.identifier.epage134en_US
dc.identifier.isiWOS:000262917300028-
dc.publisher.placeNetherlandsen_US
dc.identifier.issnl0009-8981-

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