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Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
Rong W, Chen X, Zhao K, Liu Y, Liu X, Ha S, Liu W, Kang X, Sheng X, Zhao C. Rong W, et al. Among authors: zhao k, zhao c. PLoS One. 2014 May 15;9(5):e97808. doi: 10.1371/journal.pone.0097808. eCollection 2014. PLoS One. 2014. PMID: 24831256 Free PMC article.
Molecular genetic testing in clinical diagnostic assessments that demonstrate correlations in patients with autosomal recessive inherited retinal dystrophy.
Liu X, Xiao J, Huang H, Guan L, Zhao K, Xu Q, Zhang X, Pan X, Gu S, Chen Y, Zhang J, Shen Y, Jiang H, Gao X, Kang X, Sheng X, Chen X, Zhao C. Liu X, et al. Among authors: zhao k, zhao c. JAMA Ophthalmol. 2015 Apr;133(4):427-36. doi: 10.1001/jamaophthalmol.2014.5831. JAMA Ophthalmol. 2015. PMID: 25611614
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