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Year | Number of Results |
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2011 | 2 |
2023 | 1 |
2024 | 0 |
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Mini-Review: Clinical Features and Management of Granular Corneal Dystrophy Type 2.
Korean J Ophthalmol. 2023 Aug;37(4):340-347. doi: 10.3341/kjo.2023.0032. Epub 2023 Jun 19.
Korean J Ophthalmol. 2023.
PMID: 37336511
Free PMC article.
Granular corneal dystrophy type 2 (GCD2) is an autosomal dominant corneal stromal dystrophy that is caused by p.Arg124His mutation of transforming growth factor beta induced (TGFBI) gene. It is characterized by well demarcated granular shaped opacities …
Granular corneal dystrophy type 2 (GCD2) is an autosomal dominant corneal stromal dystrophy that is caused by p. …
Genotype-phenotype correlations in Chinese patients with TGFBI gene-linked corneal dystrophy.
Long Y, Gu YS, Han W, Li XY, Yu P, Qi M.
Long Y, et al.
J Zhejiang Univ Sci B. 2011 Apr;12(4):287-92. doi: 10.1631/jzus.B1000154.
J Zhejiang Univ Sci B. 2011.
PMID: 21462384
Free PMC article.
In this paper, we report the clinical and molecular features of the distinct TGFBI (human transforming growth factor beta-induced, OMIM No. 601692) gene-linked corneal dystrophy. Altogether, five pedigrees and ten unrelated individuals diagnosed as corneal …
In this paper, we report the clinical and molecular features of the distinct TGFBI (human transforming growth factor beta-induced, OMIM No. …
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Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of Avellino corneal dystrophy.
Lisch W, Moller HU.
Lisch W, et al.
Cornea. 2011 Aug;30(8):949; author reply 949-50. doi: 10.1097/ICO.0b013e3182031e5c.
Cornea. 2011.
PMID: 21617530
No abstract available.
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