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Q28941779-122B43A2-09B1-405D-A4D0-22B1A91125B7
Q28941779-122B43A2-09B1-405D-A4D0-22B1A91125B7
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Statement
http://www.wikidata.org/entity/statement/Q28941779-122B43A2-09B1-405D-A4D0-22B1A91125B7
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger Syndrome
P2860
Q28941779-122B43A2-09B1-405D-A4D0-22B1A91125B7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28941779-122B43A2-09B1-405D-A4D0-22B1A91125B7
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type
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Statement
wasDerivedFrom
603cdec3936ddd03b79e225428f12dd18930e069
P2860
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development