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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 | ||
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===References=== | ===References=== | ||
<biblio> | <biblio> | ||
moss pmid=17470695 | |||
</biblio> | </biblio> | ||