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Q24296675-F17E4CF8-E9B3-40FA-8555-647E1F1DF3AC
Q24296675-F17E4CF8-E9B3-40FA-8555-647E1F1DF3AC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24296675-F17E4CF8-E9B3-40FA-8555-647E1F1DF3AC
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene
P1433
Q24296675-F17E4CF8-E9B3-40FA-8555-647E1F1DF3AC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24296675-F17E4CF8-E9B3-40FA-8555-647E1F1DF3AC
rank
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type
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Statement
wasDerivedFrom
dfe4998bb5bee24d554f4761934355861f16ada5
P1433
American Journal of Ophthalmology