Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATPchannel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period-Reference-Cited by-同舟云学术

Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATPchannel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period

Published:2007-11 Issue:s2 Volume:9 Page:28-39
ISSN:1462-8902
Container-title:Diabetes, Obesity and Metabolism
language:en
Short-container-title:Diabetes Obes Metab

Author:

Patch A. M.,Flanagan S. E.,Boustred C.,Hattersley A. T.,Ellard S.

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1463-1326.2007.00772.x/fullpdf

Reference44 articles.

1. HLA Genotyping Supports a Nonautoimmune Etiology in Patients Diagnosed With Diabetes Under the Age of 6 Months

2. Permanent diabetes mellitus in the first year of life

3. Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetes.

4. Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation

5. 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

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