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2
Q35204968-A76467F1-CF14-4E6E-8CD5-2DB941430D11
Q35204968-A76467F1-CF14-4E6E-8CD5-2DB941430D11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35204968-A76467F1-CF14-4E6E-8CD5-2DB941430D11
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
P2860
Q35204968-A76467F1-CF14-4E6E-8CD5-2DB941430D11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35204968-A76467F1-CF14-4E6E-8CD5-2DB941430D11
rank
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type
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Statement
wasDerivedFrom
2bff12dd5fe4c911f4e0ddf75aaa7ceafea4a659
P2860
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.