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Q37343515-34D0DEAA-602E-44D3-80EA-DA920BAF0F0B
Q37343515-34D0DEAA-602E-44D3-80EA-DA920BAF0F0B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37343515-34D0DEAA-602E-44D3-80EA-DA920BAF0F0B
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India
P2860
Q37343515-34D0DEAA-602E-44D3-80EA-DA920BAF0F0B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37343515-34D0DEAA-602E-44D3-80EA-DA920BAF0F0B
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Statement
wasDerivedFrom
9b0f49b7f66408510921f6353760550b9b5071fa
P2860
Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis.