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1.Heterozygozity for a novel FGG Trp253Cys mutation causes hypofibrinogenaemia by specifically impairing fibrinogen secretion

Heterozygozity for a novel FGG Trp253Cys mutation causes hypofibrinogenaemia by specifically impairing fibrinogen secretion / D. Vu ... [et al.] . Interná medicína : recenzovaný, postgraduálne zameraný odborný lekársky časopis. - ISSN 1335-8359 . - Roč. 6, supl. 2, č. 10 (2006), s. 38S

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