Compound heterozygous mutations in CYP1B1 gene leads to severe primary congenital glaucoma phenotype Journal title: International Journal of Ophthalmology Authors: Xian Yang Subject(s):
MUTATIONS OF THE HUMAN CYP1B1 GENE IN PATIENTS WITH PRIMARY CHILDHOOD GLAUCOMA'S IN NIGERIA. Journal title: European Journal of Biomedical and Pharmaceutical Sciences Authors: Kooffreh Mary Subject(s):
