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Coagulation Factor XIII-A A614T gene Variation is Suggestive of Founder Effect in Iranian Patients with Severe Congenital Factor XIII Deficiency

Author(s):
Majid NaderiMajid Naderi1, Shadi TabibianShadi Tabibian2, Shaban AlizadeShaban Alizade2, Zahra Sadat AbtahiZahra Sadat Abtahi3, Akbar DorgalalehAkbar Dorgalaleh4,*
1Department of Pediatrics Hematology & Oncology, Ali Ebn-e-Abitaleb Hospital Research Center for Children and Adolescents Health [RCCAH], ZahedanUniversity of Medical Sciences, Zahedan, Iran
2epartmentof Hematologyand Blood Transfusion, Allied Medical School, TehranUniversity of Medical Sciences, Tehran, Iran
3Departmentof Hematologyand Blood Transfusion, Allied Medical School, TehranUniversity of Medical Sciences, Tehran, Iran
4Department ofHematology and Blood Transfusion,School of Allied Medical Sciences,Iran University of Medical Sciences,Tehran, Iran.


Journal of Cellular & Molecular Anesthesia:Vol. 1, issue 1; e150242
Published online:Dec 22, 2015
Article type:Original Articles
How to Cite:Majid NaderiShadi TabibianShaban AlizadeZahra Sadat AbtahiAkbar DorgalalehCoagulation Factor XIII-A A614T gene Variation is Suggestive of Founder Effect in Iranian Patients with Severe Congenital Factor XIII Deficiency.J Cell Mol Anesth.1(1):e150242.https://doi.org/10.22037/jcma.v1i1.10638.

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