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I. Stoilov, A. Nurten and M. Sarfarazi, “Identification of Three Different Truncating Mutations in Cytochrome P4501B1 (CYP1B1) as the Principal Cause of Primary Congenital Glaucoma in Families Linked to the GLC3A on Chromosome 2p21,” Human Molecular Genetics, Vol. 6, No. 4, 1997, pp. 641-647. doi:10.1093/hmg/6.4.641

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