Funder
National Natural Science Foundation of China
the National Basic Research Priorities Program of China
the Zhejiang Provincial Public Welfare Technology Applied Research Project , China
Publisher
Zhejiang University Press
Subject
General Pharmacology, Toxicology and Pharmaceutics,General Veterinary,General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference26 articles.
1. Adzhubei I, Jordan DM, Sunyaev SR, 2013. Predicting functional effect of human missense mutations using polyphen–2. Curr Protoc Hum Genet, 76(1):7.20.1–7.20.41. https://doi.org/10.1002/0471142905.hg0720s76
2. Babanejad M, Fattahi Z, Bazazzadegan N, et al., 2012. A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. Am J Med Genet A, 158A(10):2485–2492. https://doi.org/10.1002/ajmg.a.35572
3. Chasman D, Adams RM, 2001. Predicting the functional consequences of non–synonymous single nucleotide polymorphisms: structure–based assessment of amino acid variation. J Mol Biol, 307(2):683–706. https://doi.org/10.1006/jmbi.2001.4510
4. Chishti MS, Bhatti A, Tamim S, et al., 2008. Splice–site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families. J Hum Genet, 53(2):101–105. https://doi.org/10.1007/s10038–007–0209–3
5. Dror AA, Avraham KB, 2009. Hearing loss: mechanisms revealed by genetics and cell biology. Annu Rev Genet, 43:411–437. https://doi.org/10.1146/annurev–genet–102108–134135
Cited by
5 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