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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433271/
https://www.ncbi.nlm.nih.gov/pubmed/25978063
http://dx.doi.org/10.1371/journal.pone.0127147

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433271/
https://www.ncbi.nlm.nih.gov/pubmed/25978063
http://dx.doi.org/10.1371/journal.pone.0127147

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