LQT6: Difference between revisions
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==Overview== | ==Overview== | ||
==LQT6 Subtype== | |||
[[LQT6]] is an [[autosomal dominant]] relatively uncommon form of LQTS. It involves mutations in the gene KCNE2 which encodes for the potassium channel beta subunit MiRP1, constituting part of the I<sub>Kr</sub> repolarizing K<sup>+</sup> current. | |||
==References== | ==References== | ||
Revision as of 16:50, 7 October 2012
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Long QT Syndrome Microchapters |
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LQT6 On the Web |
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American Roentgen Ray Society Images of LQT6 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]
Overview
LQT6 Subtype
LQT6 is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE2 which encodes for the potassium channel beta subunit MiRP1, constituting part of the IKr repolarizing K+ current.