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Kaul H 1
Showing records 1 to 1 | Display all abstracts from Kaul H78827 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
Afzal R; Firasat S; Kaul H; Ahmed B; Siddiqui SN; Zafar SN; Shahzadi M; Afshan K
Congenital anomalies 2019; 59: 152-161
