Investigation of mutational spectrum in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma

OBJECTIVE: To identify the genetic variants in the CYP1B1 gene associated with Primary Congenital Glaucoma (PCG) and to predict its pathological effect. METHOD: A descriptive study was conducted in the time period of nine months (September 2021-May 2022) after the ethical approval was taken from The...

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Detalles Bibliográficos
Autores principales: Zahid, Tazeen, Khan, Muhammad Umer, Zulfiqar, Aymn, Jawad, Fatima, Saleem, Anosh, Khan, Ahmad Raza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025705/
https://www.ncbi.nlm.nih.gov/pubmed/36950438
http://dx.doi.org/10.12669/pjms.39.2.7081

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025705/
https://www.ncbi.nlm.nih.gov/pubmed/36950438
http://dx.doi.org/10.12669/pjms.39.2.7081

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