{"product_id":"non-syndromic-autosomal-recessive-deafness-due-to-gjb2-gene-mutations-von-fadel-sharif-badria-essammak","title":"Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations","description":"\u003cp\u003eThe ubiquity of GJB2-associated hearing loss around the world is notable for a highly prevalent genetic disease. This work confirms the significant contribution of GJB2 gene mutations, particularly c.35delG, c.235delC and c.-23+1G\u0026gt;A, to congenital hearing loss in Gaza strip children and serves as both a reference for clinicians working up and counseling. Patients with congenital autosomal recessive non-syndromic hearing loss.\u003c\/p\u003e\u003cdiv class=\"aw-variant-hidden-subtitle-div\" id=\"aw-variant-subtitle-9783659803796\"\u003e\u003ch3\u003e\u003c\/h3\u003e\u003c\/div\u003e","brand":"Libri","offers":[{"title":"Softcover - 9783659803796","offer_id":39449861914717,"sku":"9783659803796","price":35.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0940\/0622\/files\/f90b0de2-e2cc-460c-a642-89333e08e704.jpg?v=1773811723","url":"https:\/\/shop.autorenwelt.de\/products\/non-syndromic-autosomal-recessive-deafness-due-to-gjb2-gene-mutations-von-fadel-sharif-badria-essammak","provider":"Autorenwelt Shop","version":"1.0","type":"link"}