Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations-Reference-Cited by-同舟云学术

Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations

Published:2020-07-08 Issue:5 Volume:42 Page:619-627
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Tavasoli Behnaz¹,Safa Majid¹²,Dorgalaleh Akbar¹,Ghasemi Jahan B.³,Rezaei Makhouri Farahnaz³,Rezvani Mohammad R.¹,Ahmadi Abbas⁴,Tabibian Shadi¹⁵,Jazebi Mohammad⁵,Baghaipour Mohammad R.⁵,Zaker Farhad¹²^ORCID

Affiliation:

1. Department of Hematology and Blood Banking Faculty of Allied Medicine Iran University of Medical Sciences Tehran Iran

2. Cellular & Molecular Research Center Iran University of Medical Sciences Tehran Iran

3. Department of Chemistry Faculty of Sciences University of Tehran Tehran Iran

4. Cellular & Molecular Research Center Kurdistan University of Medical Sciences Sanandaj Iran

5. Iranian Comprehensive Hemophilia Care Center Tehran Iran

Funder

Iran University of Medical Sciences

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13258

Reference31 articles.

1. Structural and functional changes of fibrinogen due to aging

2. Fibrinogen and Fibrin in Hemostasis and Thrombosis

3. Polymerization of fibrin: specificity, strength, and stability of knob-hole interactions studied at the single-molecule level

4. Molecular Mechanisms, Thermodynamics, and Dissociation Kinetics of Knob-Hole Interactions in Fibrin

5. Fibrinogen: biochemistry, epidemiology and determinants

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