使用患者来源的诱导多能干细胞研究 NAA10 遗传变异引起的长 QT 综合征。
关键词: Cav1.2 calcium channel NAA10 iPSC long QT rare disease
Mesh : Humans Induced Pluripotent Stem Cells Long QT Syndrome / diagnosis genetics Phenotype Myocytes, Cardiac Mutation N-Terminal Acetyltransferase A / genetics N-Terminal Acetyltransferase E / genetics
来 源:
DOI:10.1161/CIRCULATIONAHA.122.061864
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