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Title

Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization

Authors
Amri, Y
Jouini, H
Becheur, M
Dabboubi, R
Mahjoub, B
Messaoud, T
Sfar, M T
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Published in Haemophilia. 2017, vol. 23, no. 4, p. e340-e347
Abstract Congenital dysfibrinogenemia is a rare qualitative fibrinogen deficiency. Molecular defects that result in dysfibrinogenemia are usually caused by mutations which affect fibrinopeptide release, fibrin polymerization, fibrin cross-linking or fibrinolysis.
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PMID: 28594476
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Structures
Research groups Bases moléculaires des anomalies génétiques de l'hémostase (504)
Geneva Platelet Group (13)
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(ISO format)
AMRI, Y et al. Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization. In: Haemophilia, 2017, vol. 23, n° 4, p. e340-e347. https://archive-ouverte.unige.ch/unige:99479

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Deposited on : 2017-11-22

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