Clinical phenotype and genetic analysis of patients with left ventricular noncompaction caused by the biallelic mutation of MYBPC3 and MYH7

被引：0

作者：

张亚辉

机构：

[1] Capital Med Univ

[2] Beijing Anzhen Hosp

[3] Coronary Artery Dis Center

[4] Dept Acute Coronary Syndrome Ward

来源：

ChinaMedicalAbstracts(InternalMedicine) | 2024年 / 41卷 / 01期

关键词：

D O I：

暂无

中图分类号：

R542.2 [心肌疾病];

学科分类号：

摘要：

Objective To explore the relationship between pathogenic gene,mutation and phenotype of left ventricular noncompaction (LVNC) patients and their family members.Methods The subjects were the proband with LVNC and her family members.The medical history including electrocardiogram,echocardiography and cardiac magnetic resonance examination of the proband and family members was collected.

引用

页码：38 / 38

页数：1

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