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

2.50
Hdl Handle:
http://hdl.handle.net/11287/620483
Title:
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.
Authors:
Haliloglu, B.; Hysenaj, G.; Atay, Z.; Guran, T.; Abalı, S.; Turan, S.; Bereket, A.; Ellard, Sian ( 0000-0002-7620-5526 )
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:
Wiley
Journal:
Clinical endocrinology
Issue Date:
Sep-2016
URI:
http://hdl.handle.net/11287/620483
DOI:
10.1111/cen.13121
PubMed ID:
27256595
Additional Links:
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.
Type:
Journal Article
Language:
en
ISSN:
1365-2265
Appears in Collections:
Molecular Genetics; 2016 RD&E publications

Full metadata record

DC FieldValue Language
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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