Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))

B. A. Bejjani, D. W. Stockton, R. A. Lewis, K. F. Tomey, D. K. Dueker, M. Jabak, W. F. Astle, J. R. Lupski

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