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

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Publication date

2002-10

Authors

Vlietman, José J
Verhage, Jan
Vos, Hans L
Van Wijk, RichardISNI 0000000396677704
Remijn, Jasper A
Van Solinge, Wouter W.ORCID 0000-0003-2867-2581ISNI 0000000394265028
Brus, Frank

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DOI

https://doi.org/10.1046/j.1365-2141.2002.377910.x

Document Type

Article

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Abstract

Keywords

Afibrinogenemia/congenital, Female, Fibrinogen/genetics, Hemorrhagic Disorders/genetics, Homozygote, Humans, Infant, Newborn, Mutation/genetics, Case Reports, Letter

Citation

Vlietman, J J, Verhage, J, Vos, H L, van Wijk, R, Remijn, J A, van Solinge, W W & Brus, F 2002, 'Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene', British Journal of Haematology, vol. 119, no. 1, pp. 282-283. https://doi.org/10.1046/j.1365-2141.2002.377910.x

URI

https://dspace.library.uu.nl/handle/1874/460149