Identities and frequencies of variants in CYP1B1 causing primary congenital glaucoma in Pakistan

PURPOSE: Primary congenital glaucoma (PCG) is a clinically and genetically heterogeneous disease. The present study was undertaken to find the genetic causes of PCG segregating in 36 large consanguineous Pakistani families. METHODS: Ophthalmic examination including fundoscopy, or slit-lamp microscop...

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Detalles Bibliográficos
Autores principales: Rashid, Muhammad, Yousaf, Sairah, Sheikh, Shakeel A., Sajid, Zureesha, Shabbir, Asra S., Kausar, Tasleem, Tariq, Nabeela, Usman, Muhammad, Shaikh, Rehan S., Ali, Muhammad, Bukhari, Shazia A., Waryah, Ali M., Qasim, Muhammad, Riazuddin, Saima, Ahmed, Zubair M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6386514/
https://www.ncbi.nlm.nih.gov/pubmed/30820150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6386514/
https://www.ncbi.nlm.nih.gov/pubmed/30820150

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