about
A mutation in the CACNA1C gene leads to early repolarization syndrome with incomplete penetrance: A Chinese family study.Efficacy and Safety of Non-Vitamin K Antagonist Oral Anticoagulants in Asians With Nonvalvular Atrial Fibrillation: A Network Meta-AnalysisDecreased eGFR Is Associated With Ischemic Stroke in Patients With Dilated CardiomyopathyBrugada syndrome with SCN5A mutations exhibits more pronounced electrophysiological defects and more severe prognosis: A meta-analysis
P50
description
researcher (ORCID 0000-0001-9416-0862)
@en
name
Kui Hong
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type
label
Kui Hong
@en
prefLabel
Kui Hong
@en
P31
P496
0000-0001-9416-0862