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Statements

Subject Item
n2:RIV%2F61989592%3A15110%2F08%3A10225400%21RIV12-MSM-15110___
rdf:type
n5:Vysledek skos:Concept
dcterms:description
Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in functional defects Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in functional defects
dcterms:title
Three cases of abnormal fibrinogens: sumperk (Bbeta His67Leu), Unicov (Bbeta Three cases of abnormal fibrinogens: sumperk (Bbeta His67Leu), Unicov (Bbeta
skos:prefLabel
Three cases of abnormal fibrinogens: sumperk (Bbeta His67Leu), Unicov (Bbeta Three cases of abnormal fibrinogens: sumperk (Bbeta His67Leu), Unicov (Bbeta
skos:notation
RIV/61989592:15110/08:10225400!RIV12-MSM-15110___
n3:aktivita
n7:I
n3:aktivity
I
n3:cisloPeriodika
6
n3:dodaniDat
n13:2012
n3:domaciTvurceVysledku
n15:5489482
n3:druhVysledku
n10:J
n3:duvernostUdaju
n11:S
n3:entitaPredkladatele
n16:predkladatel
n3:idSjednocenehoVysledku
399994
n3:idVysledku
RIV/61989592:15110/08:10225400
n3:jazykVysledku
n17:eng
n3:klicovaSlova
serine; leucine; histidine; glycine; fibrinogen variant; arginine
n3:klicoveSlovo
n4:leucine n4:serine n4:fibrinogen%20variant n4:arginine n4:histidine n4:glycine
n3:kodStatuVydavatele
US - Spojené státy americké
n3:kontrolniKodProRIV
[DA687C7A2094]
n3:nazevZdroje
Thrombosis and Haemostasis
n3:obor
n8:FD
n3:pocetDomacichTvurcuVysledku
1
n3:pocetTvurcuVysledku
9
n3:rokUplatneniVysledku
n13:2008
n3:svazekPeriodika
100
n3:tvurceVysledku
Dyr, Je Kotlín, R. Suttnar, J. Smejkal, P. Sobotková, A. Pospíšilová, Dagmar Chrastinová, L. Reicheltová, Z. Salaj, P.
s:issn
0340-6245
s:numberOfPages
2
n12:organizacniJednotka
15110