Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review

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dc.contributor.author Welzel, Tatjana
dc.contributor.author Oefelein, Lea
dc.contributor.author Holzer, Ursula
dc.contributor.author Haack, Tobias
dc.contributor.author Kümmerle-Deschner, Jasmin
dc.contributor.author Müller, Amelie Johanna
dc.contributor.author Menden, Benita
dc.date.accessioned 2023-06-22T09:48:53Z
dc.date.available 2023-06-22T09:48:53Z
dc.date.issued 2022
dc.identifier.issn 2077-0383
dc.identifier.uri http://hdl.handle.net/10900/142499
dc.language.iso en de_DE
dc.publisher Mdpi de_DE
dc.relation.uri http://dx.doi.org/10.3390/jcm11154369 de_DE
dc.subject.ddc 610 de_DE
dc.title Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review de_DE
dc.type Article de_DE
utue.quellen.id 20230202000000_02099
utue.personen.roh Welzel, Tatjana
utue.personen.roh Oefelein, Lea
utue.personen.roh Holzer, Ursula
utue.personen.roh Muller, Amelie
utue.personen.roh Menden, Benita
utue.personen.roh Haack, Tobias B.
utue.personen.roh Gross, Miriam
utue.personen.roh Kuemmerle-Deschner, Jasmin B.
dcterms.isPartOf.ZSTitelID Journal of Clinical Medicine de_DE
dcterms.isPartOf.ZS-Issue 15 de_DE
dcterms.isPartOf.ZS-Volume 11 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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