The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report.
Anna YingYuanlin ZhouChunyue WangTao WangXuan ZhangShanshan WangShaofa KeYuyan BaoYang LiuFeng Wang
Published in: Frontiers in neurology (2024)
c.952G>A (rs267606810) and underscores the significance of considering CD as a potential etiology for unexplained ischemic stroke, particularly in patients with a family history of coagulation disorders.