Fibrinogen Foxton: a novel BbetaA277V mutation causing low normal plasma fibrinogen concentration
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Veröffentlicht in: | Thrombosis and haemostasis 2008-10, Vol.100 (4), p.708-710 |
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container_title | Thrombosis and haemostasis |
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creator | Davis, Ryan L Baker, Bartrum Brennan, Stephen O |
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ispartof | Thrombosis and haemostasis, 2008-10, Vol.100 (4), p.708-710 |
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language | eng |
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source | MEDLINE; Thieme Connect Journals |
subjects | Adult Blood Coagulation Disorders - blood Blood Coagulation Disorders - genetics Contusions - blood Contusions - genetics Crystallography Electrophoresis, Polyacrylamide Gel Female Fibrinogen - chemistry Fibrinogen - genetics Fibrinogen - metabolism Heterozygote Humans Point Mutation Protein Structure, Tertiary Sequence Analysis, Protein Spectrometry, Mass, Electrospray Ionization |
title | Fibrinogen Foxton: a novel BbetaA277V mutation causing low normal plasma fibrinogen concentration |
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