Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil

BACKGROUND: Primary congenital glaucoma (PCG), occurs due to the developmental defects in the trabecular meshwork and anterior chamber angle in children. PCG exhibits genetic heterogeneity and the CYP1B1 gene has been widely implicated worldwide. Despite the diverse mutation spectra, the clinical im...

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Publicado no:PLoS One
Main Authors: de Melo, Mônica Barbosa, Mandal, Anil K., Tavares, Ivan M., Ali, Mohammed Hasnat, Kabra, Meha, de Vasconcellos, José Paulo Cabral, Senthil, Sirisha, Sallum, Juliana M. F., Kaur, Inderjeet, Betinjane, Alberto J., Moura, Christiane R., Paula, Jayter S., Costa, Karita A., Sarfarazi, Mansoor, Paolera, Mauricio Della, Finzi, Simone, Ferraz, Victor E. F., Costa, Vital P., Belfort, Rubens, Chakrabarti, Subhabrata
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2015
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4433271/
https://ncbi.nlm.nih.gov/pubmed/25978063
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0127147
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