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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Jeyabalan, Nallathambi, Shetty, Rohit, Ghosh, Anuprita, Anandula, Venkata Ramana, Ghosh, Arka Subhra, Kumaramanickavel, Govindasamy
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Medknow Publications & Media Pvt Ltd 2013
Pynciau:
Symposium: Keratoconus
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3775069/
https://ncbi.nlm.nih.gov/pubmed/23925319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0301-4738.116055
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