Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene
DSpace/Manakin Repository
Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene
Vlietman, José J; Verhage, Jan; Vos, Hans L; van Wijk, Richard; Remijn, Jasper A; van Solinge, Wouter W; Brus, Frank
(2002) British Journal of Haematology, volume 119, issue 1, pp. 282 - 283
(Article)
Download/Full Text
The full text of this publication is not available.
Version on publisher website for UU-students and staff
Version on publisher website
Keywords: Afibrinogenemia/congenital, Female, Fibrinogen/genetics, Hemorrhagic Disorders/genetics, Homozygote, Humans, Infant, Newborn, Mutation/genetics, Case Reports, Letter
DOI:
https://doi.org/10.1046/j.1365-2141.2002.377910.x
ISSN: 0007-1048
Publisher: Wiley-Blackwell
(Peer reviewed)