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Paul S. Thornton
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Journal Articles

Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor

Paul S. Thornton, Courtney MacMullen, Arupa Ganguly, Eduardo Ruchelli, Linda Steinkrauss, Ana Crane, Lydia Aguilar-Bryan, Charles A. Stanley
Journal: Diabetes
Diabetes 2003;52(9):2403–2410
https://doi.org/10.2337/diabetes.52.9.2403
Published: 01 September 2003
View article titled, Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor
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Journal Articles

A Nonsense Mutation in the Inward Rectifier Potassium Channel Gene, Kir6.2, Is Associated With Familial Hyperinsulinism

Ann Nestorowicz, Nobuya Inagaki, Tohru Gonoi, Kathleen P Schoor, Beth Anne Wilson, Benjamin Glaser, Heddy Landau, Charles A Stanley, Paul S Thornton, Susumu Seino, M Alan Permutt
Journal: Diabetes
Diabetes 1997;46(11):1743–1748
https://doi.org/10.2337/diab.46.11.1743
Published: 01 November 1997
View article titled, A Nonsense Mutation in the Inward Rectifier Potassium Channel Gene, <em>Kir6.2</em>, Is Associated With Familial Hyperinsulinism
Open the PDF for A Nonsense Mutation in the Inward Rectifier Potassium Channel Gene, <em>Kir6.2</em>, Is Associated With Familial Hyperinsulinism in another window