Specific ion channel mutations underline the congenital long QT syndrome (LQTS).
特定离子通道的基因突变是产生遗传性长qt综合征的基础。
Mutations in genes for inherited LQTS are also associated with much more common drug-induced LQTS.
遗传性LQTS致病基因的突变也与很多普通药物诱导的LQTS相关。
Objective To study the clinical manifestations and gene mutations of Chinese long QT syndrome (LQTS) patients.
目的研究我国长qt综合征(LQTS)病人的临床特征和基因突变特点。
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