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- NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_assertion type Assertion NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_head.
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- NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_assertion wasDerivedFrom befree-20150227 NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_provenance.
- NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_assertion SIO_000772 16876867 NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_provenance.
- NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_assertion evidence source_evidence_literature NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_provenance.
- NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_assertion description "[A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626423.RACS06r-meDg_cnrVpy5PkcekdsdgSwXXOiOV-W4Owmk8130_provenance.