基因多态性与塞尔维亚人口中COVID-19患者的临床和生物化学参数有关

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Biljana Ljujic1,2, Nela Maksimovic3, Tatjana Damnjanovic3

  • 1Department of Genetics, Faculty of Medical Sciences, University of Kragujevac, Serbia.

Clinical nursing research
|January 9, 2025
PubMed
概括

低氧诱导因子-1α (HIF-1α) 基因变异与40岁以下的COVID-19患者的血小板数量较低有关. 特定的HIF-1A基因型可以预测2019年严重的冠状病毒疾病中的血小板缺血症.

关键词:
在 COVID-19 疫情中,在HIF-1A基因中,多态的多态化.这是 proBNP.血小板细胞减少症 (Thrombocytopenia) 是一种

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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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