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Article: Arginase deficiency with new phenotype and a novel mutation: Contemporary Summary

TitleArginase deficiency with new phenotype and a novel mutation: Contemporary Summary
Authors
Issue Date2012
Citation
Pediatric Neurology, 2012, v. 47 n. 4, p. 263-269 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/183778

 

DC FieldValueLanguage
dc.contributor.authorTsang, JPKen_US
dc.contributor.authorPoon, WLen_US
dc.contributor.authorLuk, HMen_US
dc.contributor.authorFung, CWen_US
dc.contributor.authorChing, CKen_US
dc.contributor.authorMak, CMen_US
dc.contributor.authorLam, CWen_US
dc.contributor.authorSiu, TSen_US
dc.contributor.authorTam, Sen_US
dc.contributor.authorWong, VCNen_US
dc.date.accessioned2013-06-18T04:13:48Z-
dc.date.available2013-06-18T04:13:48Z-
dc.date.issued2012en_US
dc.identifier.citationPediatric Neurology, 2012, v. 47 n. 4, p. 263-269en_US
dc.identifier.urihttp://hdl.handle.net/10722/183778-
dc.languageengen_US
dc.relation.ispartofPediatric Neurologyen_US
dc.titleArginase deficiency with new phenotype and a novel mutation: Contemporary Summaryen_US
dc.typeArticleen_US
dc.identifier.emailFung, CW: fcw1209m@hkucc.hku.hken_US
dc.identifier.emailLam, CW: ching-wanlam@pathology.hku.hken_US
dc.identifier.emailWong, VCN: vcnwong@hku.hken_US
dc.identifier.authorityLam, CW=rp00260en_US
dc.identifier.authorityWong, VCN=rp00334en_US
dc.identifier.hkuros214827en_US
dc.identifier.hkuros222696-
dc.identifier.volume47en_US
dc.identifier.issue4en_US
dc.identifier.spage263en_US
dc.identifier.epage269en_US

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