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Q28941779-1A7E0D7E-F6CB-453E-80AE-EBB2164FDD9C
Q28941779-1A7E0D7E-F6CB-453E-80AE-EBB2164FDD9C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28941779-1A7E0D7E-F6CB-453E-80AE-EBB2164FDD9C
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger Syndrome
P2860
Q28941779-1A7E0D7E-F6CB-453E-80AE-EBB2164FDD9C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28941779-1A7E0D7E-F6CB-453E-80AE-EBB2164FDD9C
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Statement
wasDerivedFrom
603cdec3936ddd03b79e225428f12dd18930e069
P2860
Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia