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Glycoconjugate Journal, ISSN 0282-0080, 12/2009, Volume 26, Issue 9, pp. 1259 - 1274
Journal Article
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 09/2014, Volume 130, Issue 5, pp. 612 - 625
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 09/2006, Volume 103, Issue 36, pp. 13333 - 13338
Journal Article
CORNEA, ISSN 0277-3740, 12/2008, Volume 27, Issue 10, pp. S1 - S42
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | GROENOUW TYPE-I | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of Francois | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 07/2016, Volume 17, Issue 1, pp. 47 - 47
Background: Macular corneal dystrophy (MCD) is a rare autosomal recessive disorder that is characterized by progressive corneal opacity that starts in early... 
CHST6 | Whole exome sequencing | Macular corneal dystrophy | African | VARIANTS | DISTINCT MUTATIONS | MISSENSE MUTATIONS | PREDICTION | RP1L1 | CARBOHYDRATE SULFOTRANSFERASE GENE | DISEASE | GENETICS & HEREDITY | FRAMEWORK | DNA-SEQUENCING DATA | KERATAN SULFATE | Gene mutations | Blindness | Physiological aspects | Corneal diseases | Genetic aspects | Research | Risk factors | Index Medicus
Journal Article
by Zhang, J and Wu, D and Li, Y and Fan, YD and Dai, YQ and Xu, JJ
AGING-US, ISSN 1945-4589, 02/2019, Volume 11, Issue 3, pp. 1019 - 1029
Macular corneal dystrophy (MCD) is an autosomal recessive disease featured by bilateral progressive stromal clouding and loss of vision, consequently... 
VIETNAMESE | CHST6 | PROTEOGLYCANS | SULFATION | macular corneal dystrophy | IMMUNOHISTOCHEMICAL EVIDENCE | CARBOHYDRATE-SULFOTRANSFERASE-6 | DISTINCT MUTATIONS | IDENTIFICATION | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | genetic variants | HETEROGENEITY | CARBOHYDRATE SULFOTRANSFERASE GENE | CHINESE PATIENTS
Journal Article
CELL, ISSN 0092-8674, 06/2001, Volume 105, Issue 7, pp. 957 - 969
Journal Article
Iranian Journal of Child Neurology, ISSN 1735-4668, 09/2010, Volume 4, Issue 2, pp. 55 - 58
Objective Macuiar Corneal Dystrophy (MCD) is a rare autosomal recessive disorder affecting the stroma of cornea. Most cases of MCD are caused by mutations in... 
Iranian patients | Carbohydrate sulfotransferase 6 gene (CHST6) | Macular Corneal Dystrophy (MCD)
Journal Article