Cargando…
Mutation Analysis of the TGFBI Gene in Consecutive Korean Patients With Corneal Dystrophies
BACKGROUND: Mutations in the transforming growth factor β-induced gene (TGFBI) are major causes of genetic corneal dystrophies (CDs), which can be grouped into TGFBI CDs. Although a few studies have reported the clinical and genetic features of Korean patients with TGFBI CD, no data are available re...
Autores principales: | Song, Ju Sun, Lim, Dong Hui, Chung, Eui-Sang, Chung, Tae-Young, Ki, Chang-Seok |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Laboratory Medicine
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390702/ https://www.ncbi.nlm.nih.gov/pubmed/25932442 http://dx.doi.org/10.3343/alm.2015.35.3.336 |
Ejemplares similares
-
TGFBI gene mutations in a Korean population with corneal dystrophy
por: Cho, Kyong Jin, et al.
Publicado: (2012) -
Reduced penetrance in familial Avellino corneal dystrophy associated with TGFBI mutations
por: Cao, Wenping, et al.
Publicado: (2009) -
Analysis of TGFBI Gene Mutations in Three Chinese Families with Corneal Dystrophy
por: Zhao, Feng, et al.
Publicado: (2019) -
A Novel Decorin Gene Mutation in Congenital Hereditary Stromal Dystrophy: A Korean Family
por: Lee, Jung Hye, et al.
Publicado: (2012) -
Molecular genetics of Chinese families with TGFBI corneal dystrophies
por: Zhang, Ting, et al.
Publicado: (2011)