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Q36803713-5A789B5F-2591-45D2-BFBD-D45FDAE7287D
Q36803713-5A789B5F-2591-45D2-BFBD-D45FDAE7287D
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http://www.wikidata.org/entity/statement/Q36803713-5A789B5F-2591-45D2-BFBD-D45FDAE7287D
Early noninvasive prenatal detection of a fetal CRB1 mutation causing Leber congenital amaurosis.
P2860
Q36803713-5A789B5F-2591-45D2-BFBD-D45FDAE7287D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36803713-5A789B5F-2591-45D2-BFBD-D45FDAE7287D
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wasDerivedFrom
e8ec48cd4f554f33285d4b2c5b3a8c05c653ca39
P2860
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene