Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy

Andrea L. VincentDavid M. MarkieBetina De KarolyiCatherine E. WheeldonDipika V. PatelChristina N. GrupchevaCharles N.J. McGhee

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Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy

机译：在独特的前膜角膜营养不良的常染色体显性谱系中排除已知的角膜营养不良基因

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《Molecular vision》 |2009年第2009期|共页
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Andrea L. VincentDavid M. MarkieBetina De KarolyiCatherine E. WheeldonDipika V. PatelChristina N. GrupchevaCharles N.J. McGhee;
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1. Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy [J] . Andrea L. VincentDavid M. MarkieBetina De KarolyiCatherine E. WheeldonDipika V. PatelChristina N. GrupchevaCharles N.J. McGhee Molecular vision . 2009,第2009期

机译：在独特的前膜角膜营养不良的常染色体显性谱系中排除已知的角膜营养不良基因
2. North-Carolina Macular dystrophy like phenotype in a three generation pedigree wit autosomal dominant inheritance and exclusion of MCRD1 [J] . Kellner Ulrich, Stohr Heidi, Budde Birgit, Investigative ophthalmology & visual science . 2019,第9期

机译：北卡罗来纳州黄斑营养不良等三代血腥机智常染色体主导遗传和排除MCRD1的表型
3. Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family [J] . Wei Cao, Ming Yan, QianYun Hao, Journal of International Medical Research . 2013,第2期

机译：常染色体显性Meesmann上皮角膜营养不良在中国家庭的keratin-3或keratin-12基因中没有外显子突变
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. Characterization of UBIAD1 and its role in Schnyder corneal dystrophy. [D] . Nickerson, Michael L. 2011

机译：UBIAD1的特征及其在施奈德角膜营养不良中的作用。
6. Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy [O] . Andrea L. Vincent, David M. Markie, Betina De Karolyi, 2009

机译：在独特的前膜角膜营养不良的常染色体显性谱系中排除已知的角膜营养不良基因
7. Exclusion of COL8A1, the gene encoding the α2(VIII) chain of type VIII collagen, as a candidate for Fuchs endothelial dystrophy and posterior polymorphous corneal dystrophy [O] . Urquhart, J E, Biswas, S, Black, G C M, 2006

机译：不包括COL8A1（编码VIII型胶原的α2（VIII）链的基因）作为Fuchs内皮营养不良和后部多形性角膜营养不良的候选基因
8. 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）

Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy

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