Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families

In this study, we investigated the geneticcause of sensorineural hearing loss in Moroccan patients and presented the importance of whole exome sequencing (WES) to identify candidate genes in two Moroccan families with profound deafness.

http://www.ijporlonline.com/article/S0165-5876(17)30337-3/fulltext?rss=yes

Source: International Journal of Pediatric Otorhinolaryngology - July 21, 2017 Category: ENT & OMF Authors: Sara Salime, Majida Charif, Amale Bousfiha, Soukaina Elrharchi, Amina Bakhchane, Hicham Charoute, Mostafa Kabine, Khalid Snoussi, Guy Lenaers, Abdelhamid Barakat Source Type: research