Non-viral and viral delivery systems for hemophilia A therapy: recent development and prospects

Author:

Zangi Ali Rajabi,Amiri Ala,Pazooki Pouya,Soltanmohammadi Fatemeh,Hamishehkar Hamed,Javadzadeh Yousef

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference183 articles.

1. Saxena K (2013) Barriers and perceived limitations to early treatment of hemophilia. J Blood Med 4:49

2. Favier RM, Lavergne J-M, Costa J-M, Caron C, Mazurier C, Viémont Ml et al (2000) Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female. Blood J Am Soc Hematol 96(13):4373–5

3. Al-ghtani SK (2020) Future of gene therapy in hemophilia. J Univ Stud Incl Res 1(1):17–32

4. Cohn EJ, Strong LE, Hughes W, Mulford D, Ashworth J, Melin ME et al (1946) Preparation and properties of serum and plasma proteins. IV. A System for the Separation into Fractions of the Protein and Lipoprotein Components of Biological Tissues and Fluids1a, b, c, d. J Am Chem Soc 68(3):459–75

5. Kasper C (2012) Judith Graham Pool and the discovery of cryoprecipitate. Haemophilia 18(6):833–835

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