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

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

doi:10.1046/j.1365-2141.2002.377910.x

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

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

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	282-283
Number of pages	2
Journal	British Journal of Haematology
Volume	119
Issue number	1
DOIs	https://doi.org/10.1046/j.1365-2141.2002.377910.x
Publication status	Published - Oct 2002

Keywords

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

Access to Document

10.1046/j.1365-2141.2002.377910.x

Cite this

@article{26818f08ff0144a086465e3fe2962fb1,

title = "Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene",

keywords = "Afibrinogenemia/congenital, Female, Fibrinogen/genetics, Hemorrhagic Disorders/genetics, Homozygote, Humans, Infant, Newborn, Mutation/genetics",

author = "Vlietman, \{Jos{\'e} J\} and Jan Verhage and Vos, \{Hans L\} and \{van Wijk\}, Richard and Remijn, \{Jasper A\} and \{van Solinge\}, \{Wouter W\} and Frank Brus",

year = "2002",

month = oct,

doi = "10.1046/j.1365-2141.2002.377910.x",

language = "English",

volume = "119",

pages = "282--283",

journal = "British Journal of Haematology",

issn = "0007-1048",

publisher = "John Wiley \& Sons Inc.",

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T1 - Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene

AU - Vlietman, José J

AU - Verhage, Jan

AU - Vos, Hans L

AU - van Wijk, Richard

AU - Remijn, Jasper A

AU - van Solinge, Wouter W

AU - Brus, Frank

PY - 2002/10

Y1 - 2002/10

KW - Afibrinogenemia/congenital

KW - Female

KW - Fibrinogen/genetics

KW - Hemorrhagic Disorders/genetics

KW - Homozygote

KW - Humans

KW - Infant, Newborn

KW - Mutation/genetics

U2 - 10.1046/j.1365-2141.2002.377910.x

DO - 10.1046/j.1365-2141.2002.377910.x

M3 - Article

C2 - 12358944

SN - 0007-1048

VL - 119

SP - 282

EP - 283

JO - British Journal of Haematology

JF - British Journal of Haematology

IS - 1

ER -