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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

✍ Scribed by Stoilov, I


Book ID
127280460
Publisher
Oxford University Press
Year
1997
Tongue
English
Weight
192 KB
Volume
6
Category
Article
ISSN
0964-6906

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