Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects-Reference-Cited by-同舟云学术

Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects

Published:2007-08 Issue:2 Volume:81 Page:375-382
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ellard Sian,Flanagan Sarah E.,Girard Christophe A.,Patch Ann-Marie,Harries Lorna W.,Parrish Andrew,Edghill Emma L.,Mackay Deborah J.G.,Proks Peter,Shimomura Kenju,Haberland Holger,Carson Dennis J.,Shield Julian P.H.,Hattersley Andrew T.,Ashcroft Frances M.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference20 articles.

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3. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes;Gloyn;N Engl J Med,2004

4. Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy;Hattersley;Diabetes,2005

5. Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations;Pearson;N Engl J Med,2006

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