A novel mutation I522N within the TGFBI gene caused lattice corneal dystrophy I

PURPOSE: To identify mutations within the TGFBI gene in a Chinese family with lattice corneal dystrophy type I (LCD I). METHODS: Genomic DNA of three affected, four unaffected family members and 50 normal individuals was extracted from peripheral leukocytes. All exons of TGFBI were amplified by poly...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Chunmei, Zeng, Guang, Lin, Hui, Li, Dandan, Zhao, Liming, Zhou, Nan, Qi, Yanhua
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786890/
https://www.ncbi.nlm.nih.gov/pubmed/19956413

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786890/
https://www.ncbi.nlm.nih.gov/pubmed/19956413

Ejemplares similares