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Long QT Syndrome: Difference between revisions
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Conclusions—This genotype–phenotype study indicates that in type-1 LQTS, mutations located in the transmembrane | Conclusions—This genotype–phenotype study indicates that in type-1 LQTS, mutations located in the transmembrane | ||
portion of the ion channel protein and the degree of ion channel dysfunction caused by the mutations are important | portion of the ion channel protein and the degree of ion channel dysfunction caused by the mutations are important | ||