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Q45944877-66841962-8B1B-4AE0-8C15-3CCF242B6630
Q45944877-66841962-8B1B-4AE0-8C15-3CCF242B6630
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45944877-66841962-8B1B-4AE0-8C15-3CCF242B6630
Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations.
P2860
Q45944877-66841962-8B1B-4AE0-8C15-3CCF242B6630
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45944877-66841962-8B1B-4AE0-8C15-3CCF242B6630
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type
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wasDerivedFrom
7bdd67a9222a906e6f757a137d4da76a7d4728cd
P2860
Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta