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Article: X-CGDbase: A database of X-CGD-causing mutations

TitleX-CGDbase: A database of X-CGD-causing mutations
Authors
Roosl, DCurnutte, JTHossle, JPLau, YLAriga, TNunoi, HDinauer, MCGahr, MSegal, AWNewburger, PEGiacca, MKeep, NHVan Zwieten, R
Issue Date1996
PublisherPergamon.
Citation
Immunology Today, 1996, v. 17 n. 11, p. 517-521 How to Cite?
AbstractX-linked chronic granulomatous disease (X-CGD) is an immunodeficiency caused by mutations in the gene coding for the β subunit of cytochrome b558. A database (X-CGDbase) of X-CGD mutations has been compiled, and its use and resultant information are discussed in this article.
Persistent Identifierhttp://hdl.handle.net/10722/80151
ISSN
0167-5699
ISI Accession Number ID
WOS:A1996VU20700007
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorRoosl, Den_HK
dc.contributor.authorCurnutte, JTen_HK
dc.contributor.authorHossle, JPen_HK
dc.contributor.authorLau, YLen_HK
dc.contributor.authorAriga, Ten_HK
dc.contributor.authorNunoi, Hen_HK
dc.contributor.authorDinauer, MCen_HK
dc.contributor.authorGahr, Men_HK
dc.contributor.authorSegal, AWen_HK
dc.contributor.authorNewburger, PEen_HK
dc.contributor.authorGiacca, Men_HK
dc.contributor.authorKeep, NHen_HK
dc.contributor.authorVan Zwieten, Ren_HK
dc.date.accessioned2010-09-06T08:03:00Z-
dc.date.available2010-09-06T08:03:00Z-
dc.date.issued1996en_HK
dc.identifier.citationImmunology Today, 1996, v. 17 n. 11, p. 517-521en_HK
dc.identifier.issn0167-5699en_HK
dc.identifier.urihttp://hdl.handle.net/10722/80151-
dc.description.abstractX-linked chronic granulomatous disease (X-CGD) is an immunodeficiency caused by mutations in the gene coding for the β subunit of cytochrome b558. A database (X-CGDbase) of X-CGD mutations has been compiled, and its use and resultant information are discussed in this article.en_HK
dc.languageengen_HK
dc.publisherPergamon.en_HK
dc.relation.ispartofImmunology Todayen_HK
dc.subject.meshAmino Acid Sequenceen_HK
dc.subject.meshDatabases, Factualen_HK
dc.subject.meshGranulomatous Disease, Chronic - geneticsen_HK
dc.subject.meshHumansen_HK
dc.subject.meshMolecular Sequence Dataen_HK
dc.subject.meshMutationen_HK
dc.subject.meshX Chromosomeen_HK
dc.titleX-CGDbase: A database of X-CGD-causing mutationsen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0167-4919&volume=17&issue=11&spage=517&epage=521&date=1996&atitle=X-CGDbase:+a+database+of+X-CGD-causing+mutationsen_HK
dc.identifier.emailLau, YL:lauylung@hkucc.hku.hken_HK
dc.identifier.authorityLau, YL=rp00361en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.pmid8961628-
dc.identifier.scopuseid_2-s2.0-0030296689en_HK
dc.identifier.hkuros21689en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0030296689&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume17en_HK
dc.identifier.issue11en_HK
dc.identifier.spage517en_HK
dc.identifier.epage521en_HK
dc.identifier.isiWOS:A1996VU20700007-
dc.identifier.scopusauthoridRoosl, D=6506434325en_HK
dc.identifier.scopusauthoridCurnutte, JT=7005867403en_HK
dc.identifier.scopusauthoridHossle, JP=6701667555en_HK
dc.identifier.scopusauthoridLau, YL=7201403380en_HK
dc.identifier.scopusauthoridAriga, T=7103205517en_HK
dc.identifier.scopusauthoridNunoi, H=7006326132en_HK
dc.identifier.scopusauthoridDinauer, MC=7005527771en_HK
dc.identifier.scopusauthoridGahr, M=7006490776en_HK
dc.identifier.scopusauthoridSegal, AW=7202309847en_HK
dc.identifier.scopusauthoridNewburger, PE=7006574543en_HK
dc.identifier.scopusauthoridGiacca, M=7005255834en_HK
dc.identifier.scopusauthoridKeep, NH=7003604750en_HK
dc.identifier.scopusauthoridVan Zwieten, R=6603844333en_HK
dc.identifier.issnl0167-5699-

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