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...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Aras Part Medical International Press
2023-04-01
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| Series: | Crescent Journal of Medical and Biological Sciences |
| Subjects: | |
| Online Access: | http://www.cjmb.org/pdf.php?id=588 |