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Q38901462-3DB3C1E6-84C6-4487-BEE3-97A225ECD606
Q38901462-3DB3C1E6-84C6-4487-BEE3-97A225ECD606
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38901462-3DB3C1E6-84C6-4487-BEE3-97A225ECD606
A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco.
P2860
Q38901462-3DB3C1E6-84C6-4487-BEE3-97A225ECD606
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38901462-3DB3C1E6-84C6-4487-BEE3-97A225ECD606
rank
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type
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wasDerivedFrom
4a89276461cc4dd5cc1f505b55c367d1b45486fd
P2860
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.