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Q37058489-D95BC51C-50D1-4E86-A3D1-F76A2B38E91C
Q37058489-D95BC51C-50D1-4E86-A3D1-F76A2B38E91C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058489-D95BC51C-50D1-4E86-A3D1-F76A2B38E91C
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
P921
Q37058489-D95BC51C-50D1-4E86-A3D1-F76A2B38E91C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058489-D95BC51C-50D1-4E86-A3D1-F76A2B38E91C
rank
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type
BestRank
Statement
P921
birth defect