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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Detalhes bibliográficos
Publicado no:PLoS Genet
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
Assuntos:
Research Article
Acesso em linha: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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