7[4]Xia JH,Liu CY,Tang BS,et al.Mutations in the gene encoding gap junction protein.beta-3 associated with autosomal dominant hearing impairment.Nat Genet,1998,20(4):370-373.
8[8]Dai P,Yu F,Han B,et al.The prevalence of the 235delC GJB2mutation in a Chinese deaf population.Genet Med,2007,9(5):283-289.
9[9]Wang QJ,Zhao YL,Rao SQ,et al.A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China.Clini Genet,2007,72(3):245-254.
10[10]Wang QJ,Li QZ,Rao SQ,et al.A novel mutation of POU3F4causes congenital profound sensorineural hearing loss in a large Chinese family.Laryngoscope,2006,116(6):944-950.
