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Q37058489-1A9A3FDF-67E0-4677-904E-3F0C887C2B4D
Q37058489-1A9A3FDF-67E0-4677-904E-3F0C887C2B4D
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http://www.wikidata.org/entity/statement/Q37058489-1A9A3FDF-67E0-4677-904E-3F0C887C2B4D
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
P2860
Q37058489-1A9A3FDF-67E0-4677-904E-3F0C887C2B4D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058489-1A9A3FDF-67E0-4677-904E-3F0C887C2B4D
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wasDerivedFrom
dd463d231eeee2d7f7616eb81a5e92ff98d566c7
P2860
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis