Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy

Mutations in genes that code for components of the Norrin-FZD4 ligand-receptor complex cause the inherited childhood blinding disorder familial exudative vitreoretinopathy (FEVR). Statistical evidence from studies of patients at risk for the acquired disease retinopathy of prematurity (ROP) suggest...

Descripción completa

Detalles Bibliográficos
Autores principales: Ngo, Michael H., Borowska-Fielding, Joanna, Heathcote, Godfrey, Nejat, Sara, Kelly, Melanie E., McMaster, Christopher R., Robitaille, Johane M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973993/
https://www.ncbi.nlm.nih.gov/pubmed/27489958
http://dx.doi.org/10.1371/journal.pone.0158320

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973993/
https://www.ncbi.nlm.nih.gov/pubmed/27489958
http://dx.doi.org/10.1371/journal.pone.0158320

Ejemplares similares