Author:
Zeraatpisheh Zahra,Sichani Ali Saber,Kamal Neda,Khamirani Hossein Jafari,Zoghi Sina,Ehsani Elham,Mohammadi Sanaz,Tabei Seyed Sajjad,Dastgheib Seyed Alireza,Tabei Seyed Mohammad Bagher,Dianatpour Mehdi
Publisher
Springer Science and Business Media LLC
Reference21 articles.
1. Azaiez H., Booth K. T., Ephraim S. S., Crone B., Black-Ziegelbein E. A., Marini R. J. et al. 2018 Genomic Landscape and Mutational Signatures of Deafness-Associated Genes. Am. J. Hum. Genet. 103, 484–497.
2. Bayazit Y. A. and Yilmaz M. 2006 An overview of hereditary hearing loss. Orl 68, 57–63.
3. Berman H. M., Westbrook J., Feng Z., Gilliland G., Bhat T. N., Weissig H. et al. 2000 The Protein Data Bank. Nucleic Acids Res. 28, 235–242.
4. Gao J., Wang Q., Dong C., Chen S., Qi Y. and Liu Y. 2015 Whole exome sequencing identified MCM2 as a novel causative gene for autosomal dominant nonsyndromic deafness in a Chinese family. PLoS One 10, 75–80.
5. Gürtler N. and Lalwani A. K. 2002 Etiology of syndromic and nonsyndromic sensorineural hearing loss. Otolaryngol. Clin. North Am. 35, 891–908.
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献