Determination of Factor II Codons Genotype in Southeastern Iranian Patients With Hereditary Deficiency of Factor II

Determination of Factor II Codons Genotype in Southeastern Iranian Patients With Hereditary Deficiency of Factor II

Objectives: Congenital prothrombin (factor II) deficiency is an inherited rare bleeding disorder with an autosomal recessive manner. The prevalence of this disorder is about one in 2000000 people in general population, but it is more common in areas with a high rate of consanguinity. To date, there...

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Bibliographic Details
Main Authors: Hamed Soleimani Samarkhazan, Shaban Alizadeh, Ziba Majidi, Zahra Kashani Khatib, Majid Naderi
Format: Article
Language:English
Published: Aras Part Medical International Press 2023-04-01
Series:Crescent Journal of Medical and Biological Sciences
Subjects:
factor ii deficiency
prothrombin
congenital bleeding disorders
blood coagulation factor
Online Access:http://www.cjmb.org/pdf.php?id=588

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