hrp0094fc4.5 | Diabetes | ESPE2021
Gokşen Damla
, Evin Ferda
, Işık Esra
, Ozen Samim
, Atik Tahir
, Ozkınay Ferda
, Akcan Neşe
, Ozkan Behzat
, Buyukinan Muammer
, Ozbek Mehmet Nuri
, Darcan Şukran
, Onay Huseyin
,
Introduction: MODY; is a rare type of diabetes that occurs clinically and genetically due to a single heterogeneous gene defect. To date, 14 different genes have been identified. In order to develop a holistic genetic diagnosis approach to monogenic DM, it is aimed to investigate molecular genetic diagnosis and responsible candidate genes with targeted new generation sequence analysis and whole exome sequencing (WES) method.Metho...