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المؤلفون: Majid Mojarrad, Javad Chezgi, Maliheh Alimardani, Atieh Eslahi, Mashsa Farjami, Mahmoud Shekari Khaniani, Sima Mansoori Derakhshan, Mohsen Rajati Haghi, Seyed Mojtaba Hosseini
المصدر: Fetal and Pediatric Pathology. 38:93-102
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Hearing loss, DNA Mutational Analysis, Cadherin Related Proteins, Nerve Tissue Proteins, Deafness, Iran, 030105 genetics & heredity, Pathology and Forensic Medicine, Iranian population, Young Adult, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, CDH23, Gene Frequency, otorhinolaryngologic diseases, Humans, Medicine, Child, Hearing Loss, Gene, Genetics, Sanger sequencing, 030219 obstetrics & reproductive medicine, Targeted mutation analysis, Myosin Heavy Chains, biology, business.industry, Genetic variants, Infant, General Medicine, Cadherins, Sulfate Transporters, Child, Preschool, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, symbols, Female, medicine.symptom, business, GJB6