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    Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.

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    URI
    http://hdl.handle.net/11287/618120
    Author
    Demirbilek, H.
    Arya, Ved B.
    Ozbek, M.N.
    Houghton, J. A. L.
    Baran, R.T.
    Akar, M.
    Tekes, S.
    Tuzun, H.
    Mackay, D. J.
    Flanagan, Sarah
    Hattersley, Andrew T.
    Ellard, Sian
    Hussain, K.
    Date
    2015-06
    Journal
    European journal of endocrinology / European Federation of Endocrine Societies
    Type
    Journal Article
    Research Support, Non-U.S. Gov't
    Publisher
    European Society of Endocrinology
    DOI
    10.1530/EJE-14-0852
    Rights
    Archived with thanks to European journal of endocrinology / European Federation of Endocrine Societies
    Metadata
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    Abstract
    Neonatal diabetes mellitus (NDM) is a rare form of monogenic diabetes and usually presents in the first 6 months of life. We aimed to describe the clinical characteristics and molecular genetics of a large Turkish cohort of NDM patients from a single centre and estimate an annual incidence rate of NDM in South-Eastern Anatolian region of Turkey.
    Citation
    Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations. 2015, 172 (6):697-705 Eur. J. Endocrinol.
    Publisher URL
    http://www.eje-online.org/cgi/pmidlookup?view=long&pmid=25755231
    Note
    This article is freely available, click on the 'Additional Link' above to access the full text.
    Collections
    • 2015 RD&E publications
    • Diabetes/Endocrine Services
    • Honorary contracts publications
    • Molecular Genetics

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