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    Clinical and genetic characteristics, management and long-term follow-Up of Turkish Patients with Congenital Hyperinsulinism.

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    URI
    http://hdl.handle.net/11287/618141
    Author
    Güven, A.
    Cebeci, A. N.
    Ellard, Sian
    Flanagan, Sarah
    Date
    2016-06-05
    Journal
    Journal of clinical research in pediatric endocrinology
    Type
    Journal Article
    Publisher
    Galenos
    DOI
    10.4274/jcrpe.2408
    Rights
    Archived with thanks to Journal of clinical research in pediatric endocrinology
    Metadata
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    Abstract
    Mutations in the KATP channel genes is the most common cause of congenital hyperinsulinism (CHI) of infancy. Our aim was to report the clinical and genetic characteristics, treatment modalities, and long-term prognosis of patients with CHI.
    Citation
    Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. 2016, 8 (2):197-204 J Clin Res Pediatr Endocrinol
    Publisher URL
    http://dx.doi.org/10.4274/jcrpe.2408
    Note
    This article is freely available online, 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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