医学
出血素质
血小板紊乱
桑格测序
血小板
突变
血小板疾病
鸟嘌呤核苷酸交换因子
基因
鸟苷三磷酸
遗传学
分子生物学
核苷酸
内科学
生物
血小板聚集
信号转导
出处
期刊:Cureus
[Cureus, Inc.]
日期:2020-11-25
被引量:1
摘要
Inherited platelet disorders (IPDs) are genetically heterogeneous rare disorders due to quantitative and/or qualitative abnormalities of the platelet.IPDs are often predisposed to significant medical complications.RAS guanyl-releasing protein-2 (RASGRP2) was recently identified as a gene affected in patients with platelet function defects and a bleeding complication.RASGRP2 codes for the protein CalDAG-GEFI RAS (guanyl-releasing protein-2), a guanine nucleotide exchange factor for small guanosine triphosphate(GTP)ase Rap1.We used Sanger sequencing to identify a novel function-disrupting homozygous mutation in RASGRP2 responsible for bleeding diathesis and platelet dysfunction in a patient.
科研通智能强力驱动
Strongly Powered by AbleSci AI