TGFBI gene mutations in a Korean population with corneal dystrophy

PURPOSE: To investigate the clinical and genetic features of Korean patients with corneal dystrophies associated with mutations in the human transforming growth factor-β-induced (TGFBI) gene. METHODS: In this study, 387 subjects (71 families and 89 individuals - 268 patients having TGFBI corneal dys...

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Detalles Bibliográficos
Autores principales: Cho, Kyong Jin, Mok, Jee Won, Na, Kyung Sun, Rho, Chang Rae, Byun, Yong Soo, Hwang, Ho Sik, Hwang, Kyu Yeon, Joo, Choun-Ki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413419/
https://www.ncbi.nlm.nih.gov/pubmed/22876129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413419/
https://www.ncbi.nlm.nih.gov/pubmed/22876129

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