Lv3
290 积分 2022-12-16 加入
SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis
3个月前
已完结
Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study
6个月前
已完结
Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study
7个月前
已完结
Pharmacogenetic Interactions Between Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism and Response to Cibenzoline in Patients With Hypertrophic Obstructive Cardiomyopathy
8个月前
已完结
Impact of β2-adrenoreceptor gene variants on cardiac cavity size and systolic function in idiopathic dilated cardiomyopathy
8个月前
已完结
Phenotypic variability of filamin C–related cardiomyopathy: Insights from a novel Dutch founder variant
11个月前
已完结
Exome sequencing as a tool for Mendelian disease gene discovery
1年前
已完结
The Rapidly Evolving Role of Titin in Cardiac Physiology and Cardiomyopathy
1年前
已完结
Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies
1年前
已完结
Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation APOB c.1468C>T
1年前
已完结
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