伊朗人口中的血液凝固障碍:系统性审查

Clinical laboratory
|August 10, 2023
PubMed
概括

血液凝固障碍,特别是XIII因子 (FXIII) 缺乏,在伊朗很普遍. 在这个人群中,c.562T>C突变是发现的最常见的遗传原因.

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