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Q49075196-8CAE60B2-BC84-48CF-A142-52D579B14CA3
Q49075196-8CAE60B2-BC84-48CF-A142-52D579B14CA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49075196-8CAE60B2-BC84-48CF-A142-52D579B14CA3
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.
P2860
Q49075196-8CAE60B2-BC84-48CF-A142-52D579B14CA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49075196-8CAE60B2-BC84-48CF-A142-52D579B14CA3
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Statement
wasDerivedFrom
15ae56cd919d24eed6e5c0cfc4666de707251476
P2860
Large genomic rearrangements within the PCDH15 gene are a significant cause of USH1F syndrome