The spectrum of HNF1A gene mutations in patients with MODY 3 phenotype and identification of three novel germline mutations in Turkish Population
Articles > Article · 2017
Authors: Emin KARACA, HÜSEYİN ONAY, Şevki ÇETİNKALP, Ayça AYKUT, Ruhsar Damla GÖKŞEN, Samim ÖZEN, Tahir ATİK, Şükran DARCAN, Ismihan Merve TEKİN, Feriştah Ferda ÖZKINAY
Diabetes & Metabolic Syndrome: Clinical Research & Reviews, Journal Indexed in SCI Expanded, International, Scopus, 2017, vol 11, pp S491-S496
DOI: 10.1016/j.dsx.2017.03.042
Summary
Background: Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes mellitus characterized by autosomal dominant inheritance, early age of onset, and pancreatic beta cell dysfunction. Heterozygous mutations in several genes may cause MODY.