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Article

Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene.

British journal of haematology - 1 Oct 2002

Vlietman José J, Verhage Jan, Vos Hans L, van Wijk Richard, Remijn Jasper A, van Solinge Wouter W, Brus Frank

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Share to Afibrinogenemia
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 12358944
DOI: 10.1046/j.1365-2141.2002.377910.x

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Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene.PMID 12358944Read ↗

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