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 micros...

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Detalhes bibliográficos
Main Authors: Muhammad Rashid, Sairah Yousaf, Shakeel A. Sheikh, Zureesha Sajid, Asra S. Shabbir, Tasleem Kausar, Nabeela Tariq, Muhammad Usman, Rehan S. Shaikh, Muhammad Ali, Shazia A. Bukhari, Ali M. Waryah, Muhammad Qasim, Saima Riazuddin, Zubair M. Ahmed
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2019-02-01
Colecção:Molecular Vision
Assuntos:
Primary congenital glaucoma
CYP1B1
Acesso em linha:http://www.molvis.org/molvis/v25/144/
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