Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes

Huiqin YangXueshan XiaoShiqiang LiGuiying MaiQingjiong Zhang

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Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes

机译：家族性渗出性玻璃体视网膜病变患者的新型TSPAN12突变及其相关表型

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《Molecular vision》 |2011年第2011期|共页
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Huiqin YangXueshan XiaoShiqiang LiGuiying MaiQingjiong Zhang;
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中图分类生物化学;
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1. Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes [J] . Li Shiqiang, Mai Guiying, Xiao Xueshan, Molecular vision . 2011,第2011期

机译：家族性渗出性玻璃体视网膜病变患者的新型TSPAN12突变及其相关表型
2. Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes [J] . Huiqin YangXueshan XiaoShiqiang LiGuiying MaiQingjiong Zhang Molecular vision . 2011,第2011期

机译：家族性渗出性玻璃体视网膜病变患者的新型TSPAN12突变及其相关表型
3. Mutations in LRP5, FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy [J] . Feng-Qin Rao, Xue-Bi Cai, Fei-Fei Cheng, Investigative ophthalmology & visual science . 2017,第5期

机译：LRP5，FZD4，TSPAN12，NDP，ZNF408或KIF11基因的突变占中国家族性渗出性玻璃体视网膜病变患者的38.7％
4. GENOTYPE-PHENOTYPE CORRELATION IN PATIENTS WITH FIBRILLIN-1 GENE MUTATIONS [C] . Christian Baumgartner, Daniela Baumgartner, Martin Eberle, Biomedical Engineering . 2005

机译：Fibrillin-1基因突变患者的基因型与表型相关性
5. Investigating Molecular Mechanisms Underlying Mild Phenotype in Friedreich Ataxia Patients with G130V Missense Mutation [D] . Clark, Elisia. 2018

机译：Friedreich共济失调患者G130V错义突变的轻度表型背后的分子机制的调查。
6. Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes [O] . Huiqin Yang, Xueshan Xiao, Shiqiang Li, 2011

机译：家族性渗出性玻璃体视网膜病变患者的新型TSPAN12突变及其相关表型
7. Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy [O] . Nikopoulos, Konstantinos, Gilissen, Christian, Hoischen, Alexander, 2010

机译：40 Mb链接间隔的新一代测序揭示了家族性渗出性玻璃体视网膜病变患者的TSPAN12突变。

Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes

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