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Q51857876-38AFD82F-E242-42F1-BE3C-0655C8E241C4
Q51857876-38AFD82F-E242-42F1-BE3C-0655C8E241C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51857876-38AFD82F-E242-42F1-BE3C-0655C8E241C4
Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severity.
P2860
Q51857876-38AFD82F-E242-42F1-BE3C-0655C8E241C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51857876-38AFD82F-E242-42F1-BE3C-0655C8E241C4
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type
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Statement
wasDerivedFrom
d1b436802ca21280fd5d9fcb525cf23e8ecf6489
P2860
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.