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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Bibliografiset tiedot
Päätekijät: Peroz, David, Rodriguez, Nicolas, Choveau, Frank, Baró, Isabelle, Mérot, Jean, Loussouarn, Gildas
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Blackwell Science Inc 2008
Aiheet:
Symposium Section Reports: Kv7 (KCNQ) Potassium Channels that are Mutated in Human Diseases
Linkit: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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