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APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans
Myopia is the most common vision disorder and the leading cause of visual impairment worldwide. However, gene variants identified to date explain less than 10% of the variance in refractive error, leaving the majority of heritability unexplained (“missing heritability”). Previously, we reported that...
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| Vydáno v: | PLoS Genet |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4551475/ https://ncbi.nlm.nih.gov/pubmed/26313004 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1005432 |
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