Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma

Mutations in the CYP1B1 gene are currently the main known genetic cause of primary congenital glaucoma (PCG), a leading cause of blindness in children. Here, we analyze for the first time the CYP1B1 genotype activity and the microscopic and clinical phenotypes in human PCG. Surgical pieces from trab...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:PLoS One
Auteurs principaux: García-Antón, María T., Salazar, Juan J., de Hoz, Rosa, Rojas, Blanca, Ramírez, Ana I., Triviño, Alberto, Aroca-Aguilar, José-Daniel, García-Feijoo, Julián, Escribano, Julio, Ramírez, José M.
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2017
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5407778/
https://ncbi.nlm.nih.gov/pubmed/28448622
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0176386
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires