المؤلفون: Hakimeh Azarafra, Marzieh Mohseni, Omid Ali Adeli, Kimia Kahrizi, Maryam Beheshtian, Farnaz Sadeghnia, Nooshin Nikzat, Mojgan Babanejad, Hossein Najmabadi

المصدر: International Journal of Pediatric Otorhinolaryngology. 104:195-199

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Ataxia, Adolescent, Mutation, Missense, Iran, 030105 genetics & heredity, Receptors, G-Protein-Coupled, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Atrophy, Exome Sequencing, medicine, Humans, Spinocerebellar Ataxias, Missense mutation, Young adult, Child, Hearing Loss, Gene, Genetic Association Studies, Exome sequencing, Genetics, business.industry, General Medicine, medicine.disease, Phenotype, Pedigree, Otorhinolaryngology, Pediatrics, Perinatology and Child Health, Spinocerebellar ataxia, Female, medicine.symptom, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255fa93c196282648250c9bced7a289b
https://doi.org/10.1016/j.ijporl.2017.11.014