Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus

BACKGROUND: The involvement of VSX1 gene for the genetic basis of keratoconus is unclear and controversial. The genetic screening of VSX1 from different ethnic populations can enlighten this subject. The aim of the present study is to investigate the role of VSX1 gene in patients with sporadic cases...

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Detalles Bibliográficos
Autores principales: Verma, Anshuman, Das, Manoranjan, Srinivasan, Muthiah, Prajna, Namperumalsamy V, Sundaresan, Periasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608990/
https://www.ncbi.nlm.nih.gov/pubmed/23506487
http://dx.doi.org/10.1186/1756-0500-6-103

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608990/
https://www.ncbi.nlm.nih.gov/pubmed/23506487
http://dx.doi.org/10.1186/1756-0500-6-103

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