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Q37343515-4A1E1B42-081F-42E8-9E14-C3BFE9C343BC
Q37343515-4A1E1B42-081F-42E8-9E14-C3BFE9C343BC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37343515-4A1E1B42-081F-42E8-9E14-C3BFE9C343BC
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India
P2860
Q37343515-4A1E1B42-081F-42E8-9E14-C3BFE9C343BC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37343515-4A1E1B42-081F-42E8-9E14-C3BFE9C343BC
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type
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wasDerivedFrom
9b0f49b7f66408510921f6353760550b9b5071fa
P2860
RPE65 gene: multiplex PCR and mutation screening in patients from India with retinal degenerative diseases