,KCNH2

Reema W Aljassar1, Qianyi Shen2, Buthaina Albash3

  • 1Department of Pediatrics, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.

Genetics in medicine open
|December 13, 2024
PubMed
概括

对KCNH2变异的功能评估证实了长QT综合征的两个家族的致病性. 这为准确的遗传诊断和改善疾病临床管理提供了关键证据.