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Q37320277-EF4B330D-F6DC-45D9-9ED5-5210DFE2F15E
Q37320277-EF4B330D-F6DC-45D9-9ED5-5210DFE2F15E
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http://www.wikidata.org/entity/statement/Q37320277-EF4B330D-F6DC-45D9-9ED5-5210DFE2F15E
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1.
P2860
Q37320277-EF4B330D-F6DC-45D9-9ED5-5210DFE2F15E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37320277-EF4B330D-F6DC-45D9-9ED5-5210DFE2F15E
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wasDerivedFrom
054aa641f6006ca74b01f07c5870cdfa46f83534
P2860
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis