dc.creator | Fernández-Vega B. | |
dc.creator | Álvarez L. | |
dc.creator | García M. | |
dc.creator | Artime E. | |
dc.creator | González Fernández A. | |
dc.creator | Fernández-Vega C. | |
dc.creator | Nicieza J. | |
dc.creator | Vega J.A. | |
dc.creator | González-Iglesias H. | |
dc.date.accessioned | 2020-09-02T22:17:32Z | |
dc.date.accessioned | 2022-11-08T20:23:40Z | |
dc.date.available | 2020-09-02T22:17:32Z | |
dc.date.available | 2022-11-08T20:23:40Z | |
dc.date.created | 2020-09-02T22:17:32Z | |
dc.date.issued | 2019 | |
dc.identifier | 40, 4, 342-349 | |
dc.identifier | 13816810 | |
dc.identifier | https://hdl.handle.net/20.500.12728/4465 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/5144947 | |
dc.language | en | |
dc.publisher | Taylor and Francis Ltd | |
dc.subject | genetic association study | |
dc.subject | Methylenetetrahydrofolate reductase (MTHFR) polymorphisms | |
dc.subject | retinal vein occlusion | |
dc.subject | Spanish population | |
dc.subject | world population review | |
dc.subject | 5,10 methylenetetrahydrofolate reductase (FADH2) | |
dc.subject | genomic DNA | |
dc.subject | methylenetetrahydrofolate reductase (NADPH2) | |
dc.subject | MTHFR protein, human | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | Article | |
dc.subject | branch retinal vein occlusion | |
dc.subject | case control study | |
dc.subject | central retina vein occlusion | |
dc.subject | clinical observation | |
dc.subject | comparative study | |
dc.subject | controlled study | |
dc.subject | diabetes mellitus | |
dc.subject | DNA sequence | |
dc.subject | dyslipidemia | |
dc.subject | female | |
dc.subject | gene frequency | |
dc.subject | gene location | |
dc.subject | genetic association | |
dc.subject | genetic risk | |
dc.subject | genetic variability | |
dc.subject | glaucoma | |
dc.subject | human | |
dc.subject | hypertension | |
dc.subject | kidney disease | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | prevalence | |
dc.subject | priority journal | |
dc.subject | retina vein occlusion | |
dc.subject | risk factor | |
dc.subject | single nucleotide polymorphism | |
dc.subject | Spaniard | |
dc.subject | thyroid disease | |
dc.subject | follow up | |
dc.subject | genetic association study | |
dc.subject | genetics | |
dc.subject | genotype | |
dc.subject | middle aged | |
dc.subject | pathology | |
dc.subject | prognosis | |
dc.subject | retina vein occlusion | |
dc.subject | Spain | |
dc.subject | very elderly | |
dc.subject | young adult | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Case-Control Studies | |
dc.subject | Female | |
dc.subject | Follow-Up Studies | |
dc.subject | Genetic Association Studies | |
dc.subject | Genotype | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Methylenetetrahydrofolate Reductase (NADPH2) | |
dc.subject | Middle Aged | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | Prognosis | |
dc.subject | Retinal Vein Occlusion | |
dc.subject | Risk Factors | |
dc.subject | Spain | |
dc.subject | Young Adult | |
dc.title | Association study of high-frequency variants of MTHFR gene with retinal vein occlusion in a Spanish population | |
dc.type | Article | |