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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Détails bibliographiques
Publié dans:PLoS Genet
Auteurs principaux: Tkatchenko, Andrei V., Tkatchenko, Tatiana V., Guggenheim, Jeremy A., Verhoeven, Virginie J. M., Hysi, Pirro G., Wojciechowski, Robert, Singh, Pawan Kumar, Kumar, Ashok, Thinakaran, Gopal, Williams, Cathy
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2015
Sujets:
Research Article
Accès en ligne: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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