Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation
Sayed Hamid Mousavi
Faculty of Medical Sciences, Department of the Clinical Biochemistry, Kateb University, Kabul, Afghanistan
Afghanistan National Charity Organization for Special Diseases (ANCOSD), Kabul, Afghanistan
Search for more papers by this authorSirous Zeinali
Iranian Molecular Medicine Network, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran
Search for more papers by this authorSeyed Alireza Mesbah-Namin
Faculty of Medical Sciences, Department of Clinical Biochemistry, Tarbiat Modares University, Tehran, Iran
Search for more papers by this authorMahmood Shams
Paramedical Faculty, Department of Laboratory Sciences, Babol University of Medical Sciences, Babol, Iran
Search for more papers by this authorCorresponding Author
Akbar Dorgalaleh
Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran
Correspondence
Akbar Dorgalaleh, Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.
Email: [email protected]
Search for more papers by this authorSayed Hamid Mousavi
Faculty of Medical Sciences, Department of the Clinical Biochemistry, Kateb University, Kabul, Afghanistan
Afghanistan National Charity Organization for Special Diseases (ANCOSD), Kabul, Afghanistan
Search for more papers by this authorSirous Zeinali
Iranian Molecular Medicine Network, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran
Search for more papers by this authorSeyed Alireza Mesbah-Namin
Faculty of Medical Sciences, Department of Clinical Biochemistry, Tarbiat Modares University, Tehran, Iran
Search for more papers by this authorMahmood Shams
Paramedical Faculty, Department of Laboratory Sciences, Babol University of Medical Sciences, Babol, Iran
Search for more papers by this authorCorresponding Author
Akbar Dorgalaleh
Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran
Correspondence
Akbar Dorgalaleh, Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.
Email: [email protected]
Search for more papers by this author
REFERENCES
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- 8Dorgalaleh A, Tabibian S, Shams M, et al. A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: Khash factor XIII. Semin Thromb Hemost. 2019; 45(01): 43–49.
- 9Dorgalaleh A, Naderi M, Hosseini M, et al, editors. Factor XIII deficiency in Iran: a comprehensive review of the literature. Semin Thromb Hemost. 2015; 41: 323–329.
- 10Dorgalaleh A, Assadollahi V, Tabibian S, Shamsizadeh M. Molecular Basis of Congenital Factor XIII Deficiency in Iran. Clin Appl Thromb Hemost. 2016; 24(2): 210–216.
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