GJB2 Mutations Screening in Autosomal Recessive Non-Syndrome Deaf Patients of Khouzestan Province

• Päätekijät: Kimia Kahrizi (Tekijä), Ali Sajjadi (Tekijä), Marzieh Mohseni (Tekijä), Yaser Riaz-el Hosseini (Tekijä), Hossein Najm-Abadi (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: University of Social Welfare and Rehabilitation Sciences, 2006-10-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

Objective: Hereditary Hearing loss (HHL) affects one in 1000-2000 newborns and more than 50% of these cases, the loss has a genetic basis. About 70% of HHL is non-syndromic with autosomal recessive forms accounting for ~85% of the genetic load. To date, more than 100 locus estimated for this kind of...