Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3 ’ splice acceptor site of intron 2.

Congenital Anomalies,Volume 0, Issue ja, -Not available-.

Source: Congenital Anomalies - October 1, 2018 Category: Genetics & Stem Cells Authors: Rabia Afzal, Sabika Firasat, Haiba Kaul, Bashir Ahmed, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Misbah Shahzadi, Kiran Afshan Source Type: research