Medical
Investigation of GJB2 and SLC26A4 genes related to pendred syndrome genetic deafness patients

Haider Majid Haider Al-Zaidi; Fatemehsadat Mousavinasab; Nika Radseresht; Ali Reza Mirzaei; Yasaman Moradi; Mohammad Mahmoudifar

Volume 3, Issue 3 , September 2023, , Pages 163-171

https://doi.org/10.55705/cmbr.2023.379262.1093

Abstract
  Deafness can occur due to damage to the ear, especially the inner ear. In other cases, the cause is a heterogeneous genetic abnormality and is caused by the changes that occur in the genes involved in the hearing process. Mutations in GJB2 and SLC26A4 genes are one of the most important causes of deafness ...  Read More

Investigation of GJB2 and SLC26A4 genes related to pendred syndrome genetic deafness patients