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

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