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

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Fingerprint

Dive into the research topics of '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))'. Together they form a unique fingerprint.

Medicine and Dentistry

Pharmacology, Toxicology and Pharmaceutical Science

Neuroscience

Immunology and Microbiology

Biochemistry, Genetics and Molecular Biology