Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.
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Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.
description
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name
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@en
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@nl
type
label
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@en
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@nl
prefLabel
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@en
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@nl
P2093
P2860
P356
P1433
P1476
Severe congenital factor XIII ...... ng to the ISTH/SSC guidelines.
@en
P2093
P2860
P304
P356
10.1111/HAE.12298
P577
2013-11-29T00:00:00Z