Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment
在伊朗遗传性听力障碍家族中鉴定SLC26A4基因突变
期刊:European Journal of Pediatrics
影响因子:2.6
doi:10.1007/s00431-008-0809-8
Kahrizi, Kimia; Mohseni, Marzieh; Nishimura, Carla; Bazazzadegan, Niloofar; Fischer, Stephanie M; Dehghani, Atefeh; Sayfati, Morteza; Taghdiri, Maryam; Jamali, Payman; Smith, Richard J H; Azizi, Fereydoun; Najmabadi, Hossein
