A novel VSX1 mutation identified in an individual with keratoconus in India

PURPOSE: To evaluate the possible role of the VSX1 gene in a group of patients from the Indian subcontinent with keratoconus. METHODS: Molecular analysis of 66 patients with a diagnosis of keratoconus, based on clinical examination and corneal topography, was carried out. DNA extraction from periphe...

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Detalles Bibliográficos
Autores principales: Paliwal, Preeti, Singh, Anuradha, Tandon, Radhika, Titiyal, Jeevan S, Sharma, Arundhati
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786886/
https://www.ncbi.nlm.nih.gov/pubmed/19956409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786886/
https://www.ncbi.nlm.nih.gov/pubmed/19956409

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