A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss
SERPINB6 的截短突变与常染色体隐性非综合征性神经性听力损失有关
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2010.04.004
Asli Sirmaci, Seyra Erbek, Justin Price, Mingqian Huang, Duygu Duman, F Başak Cengiz, Güney Bademci, Suna Tokgöz-Yilmaz, Burcu Hişmi, Hilal Ozdağ, Banu Oztürk, Sevsen Kulaksizoğlu, Erkan Yildirim, Haris Kokotas, Maria Grigoriadou, Michael B Petersen, Hashem Shahin, Moien Kanaan, Mary-Claire King, Zh