PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome - NASA/ADS

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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

Publication:: PLoS ONE
Pub Date:: April 2015
DOI:: 10.1371/journal.pone.0124409
Bibcode:: 2015PLoSO..1024409Z

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