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Christophe Girard
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Journal Articles

Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient With Permanent Neonatal Diabetes and Hemihypertrophy

Julian P.H. Shield, Sarah E. Flanagan, Deborah J. Mackay, Lorna W. Harries, Peter Proks, Christophe Girard, Frances M. Ashcroft, I. Karen Temple, Sian Ellard
Journal: Diabetes
Diabetes 2008;57(1):255–258
https://doi.org/10.2337/db07-0999
Published: 01 January 2008
View article titled, Mosaic Paternal Uniparental Isodisomy and an <em>ABCC8</em> Gene Mutation in a Patient With Permanent Neonatal Diabetes and Hemihypertrophy
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Journal Articles

Functional Effects of Mutations at F35 in the NH2-terminus of Kir6.2 (KCNJ11), Causing Neonatal Diabetes, and Response to Sulfonylurea Therapy

Peter Proks, Christophe Girard, Halvor Bævre, Pål R. Njølstad, Frances M. Ashcroft
Journal: Diabetes
Diabetes 2006;55(6):1731–1737
https://doi.org/10.2337/db05-1420
Published: 01 June 2006
View article titled, Functional Effects of Mutations at F35 in the NH<sub>2</sub>-terminus of Kir6.2 (<em>KCNJ11</em>), Causing Neonatal Diabetes, and Response to Sulfonylurea Therapy
Open the PDF for Functional Effects of Mutations at F35 in the NH<sub>2</sub>-terminus of Kir6.2 (<em>KCNJ11</em>), Causing Neonatal Diabetes, and Response to Sulfonylurea Therapy in another window
Includes: Supplementary data