Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
暂无分享,去创建一个
N. Lench | R. Mueller | M. Houseman | G. Camp | V. Newton
[1] C. Petit,et al. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. , 1997, Human molecular genetics.
[2] X. Estivill,et al. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. , 1997, Human molecular genetics.
[3] D. Kelsell,et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness , 1997, nature.
[4] P. Willems,et al. Nonsyndromic hearing impairment: unparalleled heterogeneity. , 1997, American journal of human genetics.
[5] T. Dryja,et al. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci. , 1994, Science.