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Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 9/2017, Volume 255, Issue 9, pp. 1779 - 1786
This study is to summarize the concurrent keratoconus (KC) and granular corneal dystrophy (GCD) phenotype and identify the underlying genetic cause in a... 
Medicine & Public Health | Granular corneal dystrophy | Keratoconus | KRT12 | Chinese | Ophthalmology | TGFBI | EYES | GENE | BETA-IG-H3 | OPHTHALMOLOGY | CHINESE FAMILY | Codon | Analysis | Genetic aspects | Nucleotide sequencing | DNA sequencing | Cornea | Missense mutation | Nonsense mutation | Corneal dystrophy | Mutation | Dystrophy | Index Medicus
Journal Article
Japanese Journal of Ophthalmology, ISSN 0021-5155, 5/2008, Volume 52, Issue 3, pp. 224 - 226
Journal Article
Progress in Molecular Biology and Translational Science, ISSN 1877-1173, 2015, Volume 134, pp. 73 - 78
Conference Proceeding
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