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  1. 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  
    C 3021
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  2. 2.Identification and expression of a missense mutation in FGG impairing fibrinogen secretion

    Identification and expression of a missense mutation in FGG impairing fibrinogen secretion  / Vu D. ... [et al.] .  Journal of medical genetics . - Vol. 42 (2005), s. e57   [Dokument nie je vo fonde knižnice]
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