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Q35637197-AAED1B9C-C65E-4DB9-ABE1-350128E15431
Q35637197-AAED1B9C-C65E-4DB9-ABE1-350128E15431
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Statement
http://www.wikidata.org/entity/statement/Q35637197-AAED1B9C-C65E-4DB9-ABE1-350128E15431
Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutations.
P2860
Q35637197-AAED1B9C-C65E-4DB9-ABE1-350128E15431
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35637197-AAED1B9C-C65E-4DB9-ABE1-350128E15431
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Statement
wasDerivedFrom
e7e0d2e83f0f4d551850544af57066f89abebe97
P2860
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype