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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...
Uloženo v:
| Vydáno v: | BMC Ophthalmol |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2017
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| Témata: | |
| On-line přístup: | 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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