The spectrum of HNF1A gene mutations in patients with MODY 3 phenotype and identification of three novel germline mutations in Turkish Population
Makaleler > Tam Makale · 2017
Yazarlar: 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, SCI Expanded İndekslerine Giren Dergi, Uluslararası, Scopus, 2017, cilt 11, ss S491-S496
DOI: 10.1016/j.dsx.2017.03.042
Özet
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.