Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations

AIMS/HYPOTHESIS: Dominantly acting loss-of-function mutations in the ABCC8/KCNJ11 genes can cause mild medically responsive hyperinsulinaemic hypoglycaemia (HH). As controversy exists over whether these mutations predispose to diabetes in adulthood we investigated the prevalence of diabetes in famil...

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Hlavní autoři: Kapoor, R. R., Flanagan, S. E., James, C. T., McKiernan, J., Thomas, A. M., Harmer, S. C., Shield, J. P., Tinker, A., Ellard, S., Hussain, K.
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer-Verlag 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3168751/
https://ncbi.nlm.nih.gov/pubmed/21674179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00125-011-2207-4
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