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Q36087162-9C12B419-7145-4DE7-B948-EFF06DEB7DDA
Q36087162-9C12B419-7145-4DE7-B948-EFF06DEB7DDA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36087162-9C12B419-7145-4DE7-B948-EFF06DEB7DDA
A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.
P2860
Q36087162-9C12B419-7145-4DE7-B948-EFF06DEB7DDA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36087162-9C12B419-7145-4DE7-B948-EFF06DEB7DDA
rank
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type
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Statement
wasDerivedFrom
b369068d6ead5e3f9898fed6b9268efbd2cc3d2b
P2860
PAX6 mutations reviewed