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Update of variants identified in the pancreatic β-cell KATPchannel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes

Year: 2020
Type: article
DOI: 10.1530/ey.17.2.11
Authors: De Franco E, Saint-Martin C, Brusgaard K, Knight Johnson AE, Aguilar-Bryan L, Bowman P, Arnoux JB, Larsen AR, May S, Greeley Saw, Calzada-Leon R, Harman B, Houghton JAL, Nishimura-Meguro, Laver TW, Ellard S, Del Gaudio D, Christesen HT, Bellanne-Chantelot C, Flanagan SE
Institutions: University of Exeter, Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Odense University Hospital, Hôpital Necker-Enfants Malades, University of Chicago, Instituto Nacional de Pediatria, Royal Devon & Exeter NHS Foundation Trust, Royal Devon University Healthcare NHS Foundation Trust, Mexican Social Security Institute
Language: English
Subfield: Surgery
Field: Medicine
Open Access status: closed
Funders: American Diabetes Association, Wellcome Trust, Kovler Family Foundation, Diabetes UK, European Foundation for the Study of Diabetes, Novo Nordisk, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: KCNJ11 Diabetes: Exploring the Role of KATP Channels in the Brain, Monogenic Diabetes: Next Generation Diagnosis, Treatment and Complications, G3016897815, Re-Engineering Translational Research at the University of Chicago, G4376901078, Incretin Regulation of Insulin Secretion in Human Neonatal Diabetes, Assessing the glycaemic and CNS response to sulphonylurea therapy in patients with KCNJ11 mutations., G6274886271, Applying the power of genetics to increase knowledge of underlying mechanisms of recessively inherited congenital hyperinsulinism., G7405478752, G9000001850, G9000334782, Diabetes Research and Training Center
OpenAlex ID: W3097190086
FWCI: 0.228
Cites: 69
Cited by: 1
Related to: 10