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Q27003290-4B563B7C-EB0D-43CB-95DC-6297E571FE50
Q27003290-4B563B7C-EB0D-43CB-95DC-6297E571FE50
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27003290-4B563B7C-EB0D-43CB-95DC-6297E571FE50
Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature
P2860
Q27003290-4B563B7C-EB0D-43CB-95DC-6297E571FE50
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27003290-4B563B7C-EB0D-43CB-95DC-6297E571FE50
rank
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Statement
wasDerivedFrom
7047987c51318ecd191ff5d76baaaa998ea13b20
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis