Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency

Author:

Abdallah Hejer Elmahmoudi,Gouider Emna,Stambouli Nejla,Amor Mohamed Ben,Jlizi Asma,Belhedi Nejla,Sassi Rim,Khodjetelkhil Houssein,Meddeb Balkis,Hafsia Raouf,Hamza Adel,Elgaaied Amel Benammar

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference8 articles.

1. Congenital factor V deficiency (parahemophilia) with true hemophilia in two brothers;Oeri;Bibliotheca Paediatrica,1954

2. Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex;Zhang;Nat. Genet.,2003

3. ERGIC-53 and traffic in the secretory pathway;Hauri;J. Cell Sci.,2000

4. Genotype-phenotype correlation in combined deficiency of factor V and factor VIII;Zhang;Blood,2008

5. D. van der Spoel GROMACS 3.0: a package for molecular simulation and trajectory analysis;Lindahl;J. Mol. Model,2001

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