Phenotype, genotype and glycaemic variability in people with activating mutations in the ABCC 8 gene: response to appropriate therapy

Activating mutations in ABCC8 are a rare cause of diabetes mellitus that manifests first in adolescence and early adulthood, with phenotype variability among family members. We report on the successful switch to sulfonylureas after chronic insulin use in participants with activating mutations in ABC...

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Veröffentlicht in:	Diabetic medicine 2020-05, Vol.37 (5), p.876-884
Hauptverfasser:	Reilly, F., Sanchez‐Lechuga, B., Clinton, S., Crowe, G., Burke, M., Ng, N., Colclough, K., Byrne, M. M.
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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