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Q30040543-1585A9FE-D16B-48F0-BCF3-34B62D4E789B
Q30040543-1585A9FE-D16B-48F0-BCF3-34B62D4E789B
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Statement
http://www.wikidata.org/entity/statement/Q30040543-1585A9FE-D16B-48F0-BCF3-34B62D4E789B
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome
P2860
Q30040543-1585A9FE-D16B-48F0-BCF3-34B62D4E789B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30040543-1585A9FE-D16B-48F0-BCF3-34B62D4E789B
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wasDerivedFrom
acbd8f57b3fdc2a1cd4d5facd21ec902c10fa6e4
P2860
Mutational analysis of the human MESP1 gene in patients with congenital heart disease reveals a highly variable sequence in exon 1.