Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report

Mutations of the WFS1 gene are responsible for most cases of Wolfram syndrome (WS), a rare, recessively inherited neurodegenerative disorder characterized by juvenile-onset non-autoimmune diabetes mellitus and op...

Source: BMC Medical Genetics - January 14, 2020 Category: Genetics & Stem Cells Authors: Maryam Sobhani, Mohammad Amin Tabatabaiefar, Soudeh Ghafouri-Fard, Asadollah Rajab, Asal Hojat, Abdol-Mohammad Kajbafzadeh and Mohammad Reza Noori-Daloii Tags: Case report Source Type: research