Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

3 results

Results by year

Filters applied: . Clear all
Page 1
Mini-Review: Clinical Features and Management of Granular Corneal Dystrophy Type 2.
Chang MS, Jun I, Kim EK. Chang MS, et al. 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. …