Long QT syndrome type 6 (Q85874): Difference between revisions
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Latest revision as of 11:14, 15 August 2026
This 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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1998894476 |
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| English | Long QT syndrome type 6 |
This 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. |
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CID11:ID_1998894476
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dki-india-ID_1998894476
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Concluído
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13 August 2026
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