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Kv7.1 (KCNQ1) properties and channelopathies
KCNQ1 is the pore-forming subunit of a channel complex whose expression and function have been rather well characterized in the heart. Almost 300 mutations of KCNQ1 have been identified in patients and a vast majority of the described mutations are linked to the long QT syndrome. Only a few mutation...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Blackwell Science Inc
2008
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2375722/ https://ncbi.nlm.nih.gov/pubmed/18174212 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2007.148254 |
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