共 129 条
[1]
Friedman TB(2003)Human nonsyndromic sensorineural deafness Annu Rev Genom Hum Genet 4 341-402
[2]
Griffith AJ(2002)CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness Am J Hum Genet 71 262-275
[3]
Astuto LM(2005)High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss Orphanet J Rare Dis 10 60-605
[4]
Bork JM(2016)Discovery of CDH23 as a significant contributor to progressive postlingual sensorineural hearing loss in Koreans PLoS One 11 e0165680-188
[5]
Weston MD(2010)Critical evaluation of the Newcastle–Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses Eur J Epidemiol 25 603-748
[6]
Askew JW(1986)Meta-analysis in clinical trials Control Clin Trials 7 177-344
[7]
Fields RR(1959)Statistical aspects of the analysis of data from retrospective studies of disease J Natl Cancer Inst 22 719-564
[8]
Orten DJ(2007)Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss Clin Genet 72 339-31
[9]
Mizutari K(2012)Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study PLoS One 7 e40366-572
[10]
Mutai H(2013)Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study Orphanet J Rare Dis 8 172-112