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

dc.contributor.authorHaliloglu, B.en
dc.contributor.authorHysenaj, G.en
dc.contributor.authorAtay, Z.en
dc.contributor.authorGuran, T.en
dc.contributor.authorAbalı, S.en
dc.contributor.authorTuran, S.en
dc.contributor.authorBereket, A.en
dc.contributor.authorEllard, Sianen
dc.date.accessioned2017-11-02T11:33:53Z
dc.date.available2017-11-02T11:33:53Z
dc.date.issued2016-09
dc.identifier.citationGCK 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)en
dc.identifier.issn1365-2265
dc.identifier.pmid27256595
dc.identifier.doi10.1111/cen.13121
dc.identifier.urihttp://hdl.handle.net/11287/620483
dc.description.abstractInactivating 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.en
dc.language.isoenen
dc.publisherWileyen
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/27256595/en
dc.rightsArchived with thanks to Clinical endocrinologyen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.subject.meshAdolescent
dc.subject.meshAge of Onset
dc.subject.meshBase Sequence
dc.subject.meshBlood Glucose
dc.subject.meshChild
dc.subject.meshChild, Preschool
dc.subject.meshDiabetes Mellitus, Type 2
dc.subject.meshFemale
dc.subject.meshGlucokinase
dc.subject.meshHemoglobin A, Glycosylated
dc.subject.meshHumans
dc.subject.meshInfant
dc.subject.meshMale
dc.subject.meshMutation
dc.subject.meshPatient Selection
dc.subject.meshRisk Assessment
dc.subject.meshTurkey
dc.titleGCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.en
dc.typeJournal Articleen
dc.identifier.journalClinical endocrinologyen
dc.description.noteThis article is freely available via PubMed Central, click on the Additional Link above to access the full-text.en
dc.type.versionPublisheden


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