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The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel.pdf
The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel
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Arrhythmia Phenotype during Fetal Life Suggests LQTS Genotype Risk Stratification of Perinatal Long QT Syndrome.pdf
Arrhythmia Phenotype during Fetal Life Suggests LQTS Genotype Risk Stratification of Perinatal Long QT Syndrome
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long qt interval in turner syndrome - a high prevalence of lqts gene mutations.pdf
long qt interval in turner syndrome – a high prevalence of lqts gene mutations
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HIV Tat protein inhibits hERG K channels A potential mechanism of HIV infection induced LQTs.pdf
HIV Tat protein inhibits hERG K channels A potential mechanism of HIV infection induced LQTs
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patient with syncope and lqts carrying a mutation in the pas domain of the herg1 channel.pdf
patient with syncope and lqts carrying a mutation in the pas domain of the herg1 channel
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Genotype and Mutation Site Specific QT Adaptation during Exercise, Recovery and Postural Changes in Children with LQTS.pdf
Genotype and Mutation Site Specific QT Adaptation during Exercise, Recovery and Postural Changes in Children with LQTS
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do lqts gene single nucleotide polymorphisms alter qtc intervals at rest and during exercise stress testing.pdf
do lqts gene single nucleotide polymorphisms alter qtc intervals at rest and during exercise stress testing
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the variant hergr148w associated with lqts is a mutation that reduces current density on co-expression with the wt:与lqts的变异hergr148w是一个突变,降低电流密度与重量的共表达.pdf
the variant hergr148w associated with lqts is a mutation that reduces current density on co-expression with the wt:与lqts的变异hergr148w是一个突变,降低电流密度与重量的共表达
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Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.pdf
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations

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