Assessment of Genetic Mutations in WFS1 & CISD2 in Wolfram Syndrome Human: OJNBD- Lupine Publishers

Assessment of Genetic Mutations in WFS1 & CISD2 in Wolfram Syndrome Human by Shahin Asadi in Online Journal of Neurology and Brain Disorders in Lupine Publishers

In this study we have analyzed 30 people. 10 patients Wolfram syndrome and 20 persons control group. The genes WFS1 and CISD2, analyzed in terms of genetic mutations made. In this study, people who have genetic mutations were targeted, with nervous disorders Wolfram syndrome. In fact, of all people with Wolfram syndrome. 10 patients Wolfram syndrome had a genetic mutation in the genes WFS1 and CISD2 Wolfram syndrome. Any genetic mutations in the target genes control group did not show.

https://www.lupinepublishers.com/neurology-brain-disorders-journal/abstracts/assessment-of-genetic-mutations-in-WFS1-CISD2-in-wolfram-syndrome-human.ID.000104.php 

https://www.lupinepublishers.com/neurology-brain-disorders-journal/fulltext/assessment-of-genetic-mutations-in-WFS1-CISD2-in-wolfram-syndrome-human.ID.000104.php

https://www.lupinepublishers.com/neurology-brain-disorders-journal/pdf/OJNBD.MS.ID.000104.pdf