Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation.

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作者： Yoonhee,Kim ^[1] ; Bhoom,Suktitipat ; Lisa R,Yanek ; Nauder,Faraday ; Alexander F,Wilson ; Diane M,Becker ; Lewis C,Becker ; Rasika A,Mathias

作者单位： Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland, United States of America. ^[1]

主题词等位基因(Alleles);队列研究(Cohort Studies);外显子(Exons);女(雌)性(Female);疾病遗传易感性(Genetic Predisposition to Disease);全基因组关联研究(Genome-Wide Association Study);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);连锁不平衡(Linkage Disequilibrium);男(雄)性(Male);中年人(Middle Aged);开放读码框架(Open Reading Frames);血小板聚集(Platelet Aggregation);多态性, 单核苷酸(Polymorphism, Single Nucleotide);受体, 细胞表面(Receptors, Cell Surface)

DOI 10.1371/journal.pone.0064179

PMID 23704978

发布时间 2024-11-03

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Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation.

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Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation.

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