Journal of Pediatric Genetics

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Stoilov I, Akarsu AN, Sarfarazi M.
Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21.

Hum Mol Genet 1997;
6 (4) 641-647

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