Corpus ID: 9894338

Lysyl oxidase-like 1 gene polymorphisms in Japanese patients with primary open angle glaucoma and exfoliation syndrome

@article{Mabuchi2008LysylO1,
  title={Lysyl oxidase-like 1 gene polymorphisms in Japanese patients with primary open angle glaucoma and exfoliation syndrome},
  author={F. Mabuchi and Yoichi Sakurada and K. Kashiwagi and Z. Yamagata and H. Iijima and S. Tsukahara},
  journal={Molecular Vision},
  year={2008},
  volume={14},
  pages={1303 - 1308}
}
Purpose To assess whether lysyl oxidase-like 1 (LOXL1) polymorphisms are associated with primary open-angle glaucoma (POAG) and exfoliation syndrome (XFS). Methods Japanese patients with POAG (n=213) or XFS (n=89) and 191 control subjects were analyzed for LOXL1 polymorphisms (rs1048661: 758G/T, Arg141Leu and rs3825942: 794G/A, Gly153Asp). Demographic and clinical features of POAG patients and control subjects were compared in terms of the TT/GG compound genotype of rs1048661 and rs3825942… Expand
The association of LOXL1 polymorphisms with exfoliation syndrome/glaucoma: Meta-analysis.
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The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas.
Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort
Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma
Effects of apolipoprotein E genotypes on the development of exfoliation syndrome.
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