Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy

Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy

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Veröffentlicht in:Thrombosis and haemostasis 2006-04, Vol.95 (4), p.738-739
Hauptverfasser: Brennan, Stephen O, Mosesson, Michael W, Lowen, Robin, Siebenlist, Kevin R, Matsunaga, Alison
Format: Artikel
Sprache:eng
Schlagworte:
Adolescent
Adult
Afibrinogenemia - genetics
Amino Acid Sequence
Base Sequence
Family Health
Female
Fibrinogen - genetics
Genetic Predisposition to Disease
Humans
Male
Molecular Sequence Data
Point Mutation
Stroke - genetics
Thrombosis - genetics
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ISSN:0340-6245