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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Dades bibliogràfiques
Publicat a:PLoS Genet
Autors principals: 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
Idioma:Inglês
Publicat: Public Library of Science 2015
Matèries:
Research Article
Accés en línia: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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