Molecular genetic analysis of Type II diabetes associated m.3243A>G mitochondrial DNA mutation in a Pakistani family

Autor: Faisal Nouroz, Hasnain Zaman, Saidul Abrar, Suleman Khan, Khushi Muhammad, Nousheen Bibi

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 18, Iss 3, Pp 305-308 (2017)
Egyptian Journal of Medical Human Genetics; Vol 18, No 3 (2017); 305-308

Background Type II diabetes is the most often considered as maternally inherited disease and A>G transition at position 3243 of mitochondrial DNA (m.3243A>G) in the encoding tRNALeu (UUR) gene is thought to be strongly responsible for the pathogenesi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2c075268557a82cd828a99ff0eba2b2
https://doi.org/10.1016/j.ejmhg.2016.12.001