Cargando…
Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus
Keratoconus (KC; Mendelian Inheritance in Man (OMIM) 14830) is a bilateral, progressive corneal defect affecting all ethnic groups around the world. It is the leading cause of corneal transplantation. The age of onset is at puberty, and the disorder is progressive until the 3(rd)–4(th) decade of lif...
| Autores principales: | , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775069/ https://www.ncbi.nlm.nih.gov/pubmed/23925319 http://dx.doi.org/10.4103/0301-4738.116055 |