A point mutation c.473A > G of ITGB3 is responsible for the formation of the Woa human platelet alloantigen

dc.contributor.authorHolzwarth, Sarah T.
dc.contributor.authorStrobel, Julian
dc.contributor.authorCooper, Nina
dc.contributor.authorLeyh, Jörg
dc.contributor.authorBayat, Behnaz
dc.contributor.authorBein, Gregor
dc.contributor.authorZingsem, Jürgen
dc.contributor.authorSachs, Ulrich J.
dc.date.accessioned2022-11-01T13:43:56Z
dc.date.available2022-11-01T13:43:56Z
dc.date.issued2020
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/8013
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-7428
dc.language.isoen
dc.rightsNamensnennung - Nicht kommerziell 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subject.ddcddc:610
dc.titleA point mutation c.473A > G of ITGB3 is responsible for the formation of the Woa human platelet alloantigen
dc.typearticle
local.affiliationFB 11 - Medizin
local.source.epageE6
local.source.journaltitleTransfusion
local.source.number1
local.source.spageE5
local.source.urihttps://doi.org/10.1111/trf.15640
local.source.volume60

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