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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Endocrinol (Oxf)
Prif Awduron: Haliloglu, Belma, Hysenaj, Gerald, Atay, Zeynep, Guran, Tulay, Abalı, Saygın, Turan, Serap, Bereket, Abdullah, Ellard, Sian
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: John Wiley and Sons Inc. 2016
Pynciau:
Original Articles
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4988380/
https://ncbi.nlm.nih.gov/pubmed/27256595
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cen.13121
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