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European Journal of Paediatric Neurology, ISSN 1090-3798, 2014, Volume 19, Issue 2, pp. 176 - 180
Journal Article
HAMOSTASEOLOGIE, ISSN 0720-9355, 11/2016, Volume 36, Issue 4A, pp. S34 - S37
Afibrinogenemia represents the rarest form of fibrinogen deficiency. Causative missense mutations occur rarely and may improve the understanding of fibrinogen... 
FGB | FGA | bleeding | Fibrinogen | Afibrinogenemia | FGG | UPDATE | HEMATOLOGY
Journal Article
Journal Article
Blood, ISSN 0006-4971, 12/2002, Volume 100, Issue 13, pp. 4478 - 4484
Congenital afibrinogenemia is a rare inherited coagulopathy, characterized by very low or unmeasurable plasma levels of immunoreactive fibrinogen. So far, 25... 
FGA | A-ALPHA-CHAIN | DONOR | THROMBOSIS | TRUNCATION | HEMATOLOGY | INHERITED AFIBRINOGENEMIA
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 11/2004, Volume 12, Issue 11, pp. 891 - 898
Among rare inherited deficiencies of coagulation factors, congenital afibrinogenaemia is characterised by the lack of fibrinogen in plasma. In the last few... 
FGA | Large deletion | Fibronigen cluster | UPD | Chromosome 4 | Congenital afibrogenaemia | Short direct repeats | RECOMBINATION | MECHANISM | congenital afibrinogenaemia | BIOCHEMISTRY & MOLECULAR BIOLOGY | large deletion | IDENTIFICATION | chromosome 4 | short direct repeats | MUTATION | DISEASE | GENETICS & HEREDITY | DISOMY | SITES | fibrinogen cluster | PATIENT | SECRETION
Journal Article
Journal Article