Association of LOXL1 gene polymorphisms with exfoliation syndrome/glaucoma and primary open angle glaucoma in a Turkish population

PURPOSE: To investigate the association of lysyl oxidase like 1 (LOXL1) variants with exfoliation syndrome (XFS), exfoliation glaucoma (XFG), and primary open angle glaucoma (POAG) in a Turkish population. METHODS: Two LOXL1 single nucleotide polymorphisms (SNPs), rs1048661 (R141L) and rs3825942 (G1...

Descripción completa

Detalles Bibliográficos
Autores principales: Kasım, Burcu, İrkeç, Murat, Alikaşifoğlu, Mehmet, Orhan, Mehmet, Mocan, Mehmet Cem, Aktaş, Dilek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559092/
https://www.ncbi.nlm.nih.gov/pubmed/23378724

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559092/
https://www.ncbi.nlm.nih.gov/pubmed/23378724

Ejemplares similares