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An Entity of Type :
wikibase:Statement
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BestRank
Statement
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BestRank
Statement
OpenCitations bibliographic resource ID
1409530
psn:P3181
https://w3id.org/oc/corpus/br/1409530
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wdref:7b1512d5837a12ff741d53006bece74ebf44015e
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OpenCitations bibliographic resource ID
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A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance
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