|
rs1217691063
|
|
|
0.030 |
GeneticVariation |
BEFREE |
There were no significant differences in the genotype distributions of the ACE I/D and MTHFR C677T polymorphisms between the NAION and control groups (p=0.261 and p=0.354, respectively), whereas the genotype distribution of the G/T (Lys198Asn) polymorphism of the ET-1 gene varied significantly between the groups (p=0.009).
|
23401650 |
2013 |
|
rs1217691063
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The 12 patients with NAION were more likely than controls to demonstrate homozygosity for the methylenetetrahydrofolate reductase (MTHFR) C677T mutation (50% vs 11 %; Fisher's P =.009, with the likelihood of a type I error quite small, 0.9%).
|
15007309 |
2004 |
|
rs1217691063
|
|
|
0.030 |
GeneticVariation |
BEFREE |
These results suggest that hyperhomocyst(e)inaemia, but not MTHFR C677T mutation is associated with NAION.
|
11423453 |
2001 |
|
rs5370
|
|
|
0.010 |
GeneticVariation |
BEFREE |
There were no significant differences in the genotype distributions of the ACE I/D and MTHFR C677T polymorphisms between the NAI</span>ON and control groups (p=0.261 and p=0.354, respectively), whereas the genotype distribution of the G/T (Lys198Asn) polymorphism of the ET-1 gene varied significantly between the groups (p=0.009).
|
23401650 |
2013 |
|
rs1799983
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that eNOS G894T polymorphism is not associated with NAION occurrence as the genotype and allele frequencies were not significantly different between the control and patient groups (TT vs. GG + GT: P = 0.646 and T vs. G: P = 0.86).
|
21073768 |
2010 |
|
rs751377893
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In a 12-member, 3-generation kindred with conjoint inheritance of G1691A factor V Leiden (FVL) and G20210A prothrombin gene (PTG) mutations, identified through a proband with amaurosis fugax and his father with nonarteritic ischemic optic neuropathy (NAION), the authors' hypothesis was that ocular thrombosis was a diagnostic window to familial thrombophilia-thrombosis.
|
18796459 |
2009 |
|
rs899127658
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In a 12-member, 3-generation kindred with conjoint inheritance of G1691A factor V Leiden (FVL) and G20210A prothrombin gene (PTG) mutations, identified through a proband with amaurosis fugax and his father with nonarteritic ischemic optic neuropathy (NAION), the authors' hypothesis was that ocular thrombosis was a diagnostic window to familial thrombophilia-thrombosis.
|
18796459 |
2009 |
|
rs1188383936
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The 12 patients with NAION were more likely than controls to demonstrate homozygosity for the methylenetetrahydrofolate reductase (MTHFR) C677T mutation (50% vs 11 %; Fisher's P =.009, with the likelihood of a type I error quite small, 0.9%).
|
15007309 |
2004 |