Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient

Bei ZhangYu-Feng Yao

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Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient

机译：伴有球状变性的胶体状滴状角膜营养不良伴新的TACSTD2突变

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《Molecular vision 》 |2010年第2010期| 共页
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Bei ZhangYu-Feng Yao;
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中图分类生物化学 ;
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1. Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient [J] . Yao Yu-Feng, Zhang Bei Molecular vision . 2010 ,第2010期

机译：伴有球状变性的胶体状滴状角膜营养不良伴新的TACSTD2突变
2. A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy [J] . Jing Yang, Liu Chun, Wang Liya Molecular vision . 2009 ,第2009期

机译：在两名中国兄弟患有胶状滴状角膜营养不良中鉴定出一种新的TACSTD2突变
3. A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy [J] . Yang JingChun LiuLiya Wang Molecular vision . 2009 ,第2009期

机译：在两名中国兄弟患有胶状滴状角膜营养不良中鉴定出一种新的TACSTD2突变
4. A Simple DNA Chip for Diagnosis of Most Common Corneal Dystrophies Caused by βigh3 Gene Mutations [C] . So Young Yoo, Tae-im Kim, Sang Yup Lee, Frontiers in the Convergence of Bioscience and Information Technologies . 2007

机译：一种简单的DNA芯片，用于诊断βigh3基因突变引起的最常见的角膜营销蛋白酶
5. Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient [O] . Bei Zhang, Yu-Feng Yao 2010

机译：伴有球状变性的胶体状滴样角膜营养不良伴新的TACSTD2突变
6. Clinical and Ultrastructural Studies of Gelatinous Drop-Like Corneal Dystrophy (GDLD) of a Patient with TACSTD2 Gene Mutation [O] . Ali Masmali, Aljoharah Alkanaan, Hind M. Alkatan, 2019

机译：Tacstd2基因突变患者凝胶状滴眼岩型角膜营养镜（GDLD）的临床和超微结构研究
7. Crystalline Retinopathy (Bietti's Tapetoretinal Degeneration without Marginal Corneal Dystrophy) [R] . Mauldin, W. M., O'Connor, P. S. 1981

机译：结晶性视网膜病变（Bietti的Tapetoretinal变性没有边缘角膜营养不良）

Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient

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