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Q52641748-890A7F39-D140-4C48-BEB1-E2EE98BB9884
Q52641748-890A7F39-D140-4C48-BEB1-E2EE98BB9884
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52641748-890A7F39-D140-4C48-BEB1-E2EE98BB9884
A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis.
P2860
Q52641748-890A7F39-D140-4C48-BEB1-E2EE98BB9884
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52641748-890A7F39-D140-4C48-BEB1-E2EE98BB9884
rank
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type
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Statement
wasDerivedFrom
ec665d33d54312f0667edaff973d6ce681adb11c
P2860
Fgf8 Expression and Degradation of Retinoic Acid Are Required for Patterning a High-Acuity Area in the Retina.