شفقتی, یوسف

[ 1 ] - طیف جهش های ژن کانکسین 26 در جمعیت ناشنوایان غیر سندرمیک استان همدان

Introduction & Objective : Hearing loss is the most prevalent form of sensory impairment in humans, affecting approximately one in 1000 infants. In more than half of the cases, the deafness is inherited, and about 80% of hereditary deafness transmitted by autosomal recessive pattern. In hereditary congenital deafness, numerous mutations in GJB2 make the largest fractional contribution in many w...