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Q24319483-DD2DAB6A-6B27-4ED6-880A-A9159FFB1272
Q24319483-DD2DAB6A-6B27-4ED6-880A-A9159FFB1272
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24319483-DD2DAB6A-6B27-4ED6-880A-A9159FFB1272
A model for the molecular underpinnings of tooth defects in Axenfeld-Rieger syndrome
P2860
Q24319483-DD2DAB6A-6B27-4ED6-880A-A9159FFB1272
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24319483-DD2DAB6A-6B27-4ED6-880A-A9159FFB1272
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Statement
wasDerivedFrom
a6fdccfdd6a2c367ed71ed3f06764e999dfc7f1e
P2860
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.