Transethnic Replication of Association of CTG18.1 Repeat Expansion of TCF4 Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant

Xing Chao; Gong Xin; Hussain Imran; Khor Chiea-Chuen; Tan Donald T. H.; Aung Tin; Mehta Jodhbir S.; Vithana Eranga N.; Mootha V. Vinod

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Transethnic Replication of Association of CTG18.1 Repeat Expansion of TCF4 Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant

机译：TCG48.1基因重复扩增与Fuchs角膜营养不良症在中国的CTG18.1重复扩增相关联的跨种族复制暗示了常见的因果变异

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PURPOSE. To test the association between the CTG18.1 trinucleotide repeat expansion of TCF4 gene and Fuchs' endothelial corneal dystrophy (FECD) in a Chinese population.

机译：目的。为了测试中国人口中TCF4基因的CTG18.1三核苷酸重复扩增与Fuchs内皮角膜营养不良（FECD）之间的关联。

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《Investigative ophthalmology & visual science》 |2014年第11期|共6页
作者
Xing Chao; Gong Xin; Hussain Imran; Khor Chiea-Chuen; Tan Donald T. H.; Aung Tin; Mehta Jodhbir S.; Vithana Eranga N.; Mootha V. Vinod;
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正文语种 eng
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Fuchs' corneal dystrophy; genetic diseases; TCF4; CTG18.1 trinucleotide repeat;

机译：福克斯角膜营养不良;遗传疾病;TCF4;CTG18.1三核苷酸重复;

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1. Transethnic Replication of Association of CTG18.1 Repeat Expansion of TCF4 Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant [J] . Xing Chao, Gong Xin, Hussain Imran, Investigative ophthalmology & visual science . 2014,第11期

机译：TCG48.1基因重复扩增与Fuchs角膜营养不良症在中国的CTG18.1重复扩增相关联的跨种族复制暗示了常见的因果变异
2. Association and Familial Segregation of CTG18.1 Trinucleotide Repeat Expansion of TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy [J] . V. Vinod Mootha, Xin Gong, Hung-Chih Ku, Investigative ophthalmology & visual science . 2014,第1期

机译：Fuchs内皮角膜营养不良中TCG4基因的CTG18.1三核苷酸重复扩增的关联和家族分离
3. Association and familial segregation of CTG18.1 trinucleotide repeat expansion of TCF4 gene in fuchs' endothelial corneal dystrophy [J] . Investigative ophthalmology & visual science . 2014,第1期

机译：Fuchs内皮角膜营养不良中CTG18.1三核苷酸TCF4基因重复扩增的缔合与家族分离
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. Improving discovery of causal variants in genetic association studies [D] . Dickson, Samuel P. 2009

机译：改善遗传关联研究中因果变异的发现
6. Transethnic Replication of Association of CTG18.1 Repeat Expansion of TCF4 Gene With Fuchs Corneal Dystrophy in Chinese Implies Common Causal Variant [O] . Chao Xing, Xin Gong, Imran Hussain, -1

机译：TCG48.1基因重复扩增与Fuchs角膜营养不良症在中国的CTG18.1重复扩增关联的跨民族复制暗示了常见的因果关系
7. Association and Familial Segregation of CTG18.1 Trinucleotide Repeat Expansion ofTCF4Gene in Fuchs' Endothelial Corneal Dystrophy [O] . V. Vinod Mootha, Xin Gong, Hung-Chih Ku, 2014

机译：CTG18.1蛋白酶蛋白酶拷贝逆膨胀的关联和家族性偏析福克斯内皮角膜营养不良液中的氢气

Transethnic Replication of Association of CTG18.1 Repeat Expansion of TCF4 Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant

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