Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI-Glu555): a cross-reactive material positive variant defective in factor IX activation

Author:

Zivelin A.,Ogawa T.,Bulvik S.,Landau M.,Toomey J. R.,Lane J.,Seligsohn U.,Gailani D.

Publisher

Wiley

Subject

Hematology

Reference40 articles.

1. Human blood coagulation factor XI. Purification, properties, and mechanism of activation by activated factor XII.

2. Factor XI Deficiency

3. Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

4. 5 A Zivelin, R Yatuv, S Livnat, H Bulvik, H Peretz, O Salomon, and U Seligsohn . Severe factor XI deficiency caused by a Gly555Glu substitution encodes for a cross reacting material positive factor XI . Thromb Haemostas (Suppl.)2001 : Abstract P1111.

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1. A novel mutation (Tyr503Cys) in a severe factor XI deficiency;Blood Coagulation & Fibrinolysis;2018-04

2. Factor XI Deficiency;Textbook of Hemophilia;2014-04-24

3. Congenital Factor XI Deficiency: An Update;Seminars in Thrombosis and Hemostasis;2013-08-08

4. Factor XI: Hemostasis, Thrombosis, and Antithrombosis;Thrombosis Research;2012-05

5. A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern Italy*;European Journal of Haematology;2011-11-17

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