1Forge A, Becker D, Casalotti S, et al. Gap junctions and connexin expression in the inner ear [ J ]. Novartis Found Symp, 1999,219 : 134 - 150.
2Green GE ,Scott DA, McDonald JM, et al. Carrier rates in the midwestem United States for GJB2 mutations causing inherited deafness [ J ]. JAMA, 1999,281:2211 -2216.
3Uyguner O, Emiroglu M, Uzumcu A, et al. Frequencies of gap-and fight-junction mutations in Turkish families with autosomal-recessive non-sydromic hearing loss [ J ]. Clin Genet, 2003,64 : 65- 69.
4Andreas R, Janeeke, Almut HS, et al.Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations-phenotypic spectrum and frequencies of JGB'2 mutations in Austria [ J]. Human Genetics,2003,111 (2) :154 - 153.
5Tuija L, Marja-Lecna V, Mirja L, et al. Connexin 26 mutations and nonsyndromic hearing impairment in northem Finland[J]. Laryngoscope, 2003,113(10) : 1758 - 1763..
6Dandrea P, Veronesi V, Bicego M, et al. Heating loss: frequency and functional studies of the most common connexin 26 alleles [ J ]. Biochemical and Biophysical Research Communications,2002,296:685 - 691.
7Pampanos A, Economides J, Iliadou V,et al. Prevalence of GJB2 mutations in prelingual deafness in the Greek populationl Jl. International Journal of Pediatric Otorhinolaryngoy, 2002,65 : 101 -108.
8Kudo T, Ikeda K, Kure S, et al. Novel mutations in the connexin26 gene (GJB2) responsible for childhood deafness in the Japanese population[ J]. Am J Med Genet ,2000,90 : 141 - 145.
9Rabionet R, Zelante L, Lopez-Bigal N, et al. Molecular basis of childhood deafness resulting from mutations in the GJB2 ( connexin 26 ) gene [ J ]. Hum Genet,2000,106:40 - 44.
10DenoyeUe F, Marlin S, Wei D, et al. Clinical features of the prevalent form of childhood deafness , DFNB1, due to a connexin26 gene defect: implications for genetic counseling [ J ]. Lancet,1999,353 : 1298 - 1303.
