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Ein Fall von Muckle-Wells-Syndrom mit einer neuen NLRP3-mutation

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dc.contributor.coauthorMetz, Martin
dc.contributor.coauthorLohse, Peter
dc.contributor.coauthorKrause, Karoline
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorYüksel, Simge
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:52:22Z
dc.date.issued2018
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.1111/ddg.13640_g
dc.identifier.eissn1610-0387
dc.identifier.issn1610-0379
dc.identifier.quartileQ1
dc.identifier.urihttps://doi.org/10.1111/ddg.13640_g
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14847
dc.keywordsClinical and life sciences
dc.keywordsAuto-inflammatory diseases
dc.keywordsFamilial mediterranean fever
dc.language.isodeu
dc.publisherWiley
dc.relation.ispartofJDDG: Journal of the German Society of Dermatology/ JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT
dc.subjectDermatology
dc.titleEin Fall von Muckle-Wells-Syndrom mit einer neuen NLRP3-mutation
dc.title.alternativeEin fall von muckle-wells-syndrom mit einer neuen NLRP3-mutation
dc.typeLetter
dspace.entity.typePublication
local.contributor.kuauthorYüksel, Simge
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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