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Analysis of the VSX1 gene in sporadic keratoconus patients from China
BACKGROUND: Keratoconus normally presents as a sporadic disease. Although different studies have found sequence variants of the visual system homeobox 1 (VSX1) gene associated with keratoconus in humans, no research has detected such variants in sporadic keratoconus patients from China. To investiga...
Tallennettuna:
| Julkaisussa: | BMC Ophthalmol |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5615802/ https://ncbi.nlm.nih.gov/pubmed/28950846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-017-0567-3 |
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