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Başlık: Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations
Yazarlar: Aykut, Ayça
Karaca, Emin
Onay, Hüseyin
Gökşen, Damla
Çetinkalp, Şevki
Ersoy, Betül
Çakır, Esra Papatya
Büyükinan, Muammer
Kara, Cengiz
Anık, Ahmet
Kırel, Birgül
Özen, Samim
Atik, Tahir
Darcan, Şükran
Özkınay, Ferda
Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı/Çocuk Endokrinolojisi Bilim Dalı.
0000-0002-1684-1053
Eren, Erdal
AAH-1155-2021
AAM-1734-2020
36113153400
Anahtar kelimeler: Genetics & heredity
MODY
GCK gene
Turkish population
Glucokinase mutations
Missense mutations
Diabetes-mellitus
Young mody
Onset
Children
Identification
Diagnosis
Families
Yayın Tarihi: 30-Oca-2018
Yayıncı: Elsevier
Atıf: Aykut, A. vd. (2018). ''Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations''. Gene, 641, 186-189.
Özet: Maturity onset diabetes is a genetic form of diabetes mellitus characterized by an early age at onset and several etiologic genes for this form of diabetes have been identified in many patients. Maturity onset diabetes type 2 [MODY2 (#125851)] caused by mutations in the glucokinase gene (GCK). Although its prevalence is not clear, it is estimated that 1%-2% of patients with diabetes have the monogenic form. The aim of this study was to evaluate the molecular spectrum of GCK gene mutations in 177 Turkish MODY type 2 patients. Mutations in the GCK gene were identified in 79 out of 177. All mutant alleles were identified, including 45 different GCK mutations, 20 of which were novel.
URI: https://doi.org/10.1016/j.gene.2017.10.057
https://www.sciencedirect.com/science/article/pii/S0378111917309034
http://hdl.handle.net/11452/34691
ISSN: 0378-1119
1879-0038
Koleksiyonlarda Görünür:Scopus
Web of Science

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