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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jeyabalan, Nallathambi, Shetty, Rohit, Ghosh, Anuprita, Anandula, Venkata Ramana, Ghosh, Arka Subhra, Kumaramanickavel, Govindasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Symposium: Keratoconus
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

Internet

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

Ejemplares similares