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Kir6.1- and SUR2-dependent K(ATP) overactivity disrupts intestinal motility in murine models of Cantú syndrome

Cantú syndrome (CS), caused by gain-of-function (GOF) mutations in pore-forming (Kir6.1, KCNJ8) and accessory (SUR2, ABCC9) ATP-sensitive potassium (K(ATP)) channel subunit genes, is frequently accompanied by gastrointestinal (GI) dysmotility, and we describe 1 CS patient who required an implanted i...

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Detalles Bibliográficos
Autores principales:	York, Nathaniel W., Parker, Helen, Xie, Zili, Tyus, David, Waheed, Maham Akbar, Yan, Zihan, Grange, Dorothy K., Remedi, Maria Sara, England, Sarah K., Hu, Hongzhen, Nichols, Colin G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	American Society for Clinical Investigation 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714409/ https://www.ncbi.nlm.nih.gov/pubmed/33170808 http://dx.doi.org/10.1172/jci.insight.141443

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