Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Epilepsy and KCNJ11[original query] |
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Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype. Diabetologia 2006 Jun 49 (6): 1190-7. Flanagan S E, Edghill E L, Gloyn A L, Ellard S, Hattersley A |
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy. Epilepsy research 2015 Oct 118 22-28. Schoeler Natasha E, Leu Costin, White Jon, Plagnol Vincent, Ellard Sian, Matarin Mar, Yellen Gary, Thiele Elizabeth A, Mackay Mark, McMahon Jacinta M, Scheffer Ingrid E, Sander Josemir W, Cross J Helen, Sisodiya Sanjay |
First case of neonatal diabetes with KCNJ11 Q52R mutation successfully switched from insulin to sulphonylurea treatment. Journal of diabetes investigation 2017 1 8 (5): 716-719. Ioacara Sorin, Flanagan Sarah, Fröhlich-Reiterer Elke, Goland Robin, Fica Simo |
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