共 50 条
- [41] Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss LARYNGOSCOPE, 2004, 114 (04): : 607 - 611
- [43] Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population Journal of Human Genetics, 2015, 60 : 613 - 617
- [45] Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population Journal of Human Genetics, 2008, 53 : 1022 - 1028
- [47] Connexin26 mutations in non-syndromic hearing loss 4TH EUROPEAN CONGRESS OF OTO-RHINO-LARYNGOLOGY HEAD AND NECK SURGERY, VOLS 1 AND 2, 2000, : 121 - 124
- [49] Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria Human Genetics, 2002, 111 : 145 - 153
- [50] Functional Evaluation of GJB2 Variants in Nonsyndromic Hearing Loss Molecular Medicine, 2011, 17 : 550 - 556