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GCK gene mutations are a common cause of childhood‐onset MODY (maturity‐onset diabetes of the young) in Turkey

OBJECTIVE: Inactivating heterozygous mutations in the GCK gene are a common cause of MODY and result in mild fasting hyperglycaemia, which does not require treatment. We aimed to identify the frequency, clinical and molecular features of GCK mutations in a Turkish paediatric cohort. DESIGN AND PATIE...

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Detalles Bibliográficos
Autores principales:	Haliloglu, Belma, Hysenaj, Gerald, Atay, Zeynep, Guran, Tulay, Abalı, Saygın, Turan, Serap, Bereket, Abdullah, Ellard, Sian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2016
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988380/ https://www.ncbi.nlm.nih.gov/pubmed/27256595 http://dx.doi.org/10.1111/cen.13121

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