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

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    Open Access article (176.8Kb)
    URI
    http://hdl.handle.net/11287/620483
    Author
    Haliloglu, B.
    Hysenaj, G.
    Atay, Z.
    Guran, T.
    Abalı, S.
    Turan, S.
    Bereket, A.
    Ellard, Sian
    Date
    2016-09
    Journal
    Clinical endocrinology
    Type
    Journal Article
    Publisher
    Wiley
    DOI
    10.1111/cen.13121
    Rights
    Archived with thanks to Clinical endocrinology
    Metadata
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    Abstract
    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.
    Citation
    GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey. 2016, 85 (3):393-9 Clin. Endocrinol. (Oxf)
    Publisher URL
    https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/27256595/
    Note
    This article is freely available via PubMed Central, click on the Additional Link above to access the full-text.
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    • 2016 RD&E publications
    • Molecular Genetics

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