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Q36890893-F4E2964B-DB26-496A-A968-75D2BDE9F86F
Q36890893-F4E2964B-DB26-496A-A968-75D2BDE9F86F
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Statement
http://www.wikidata.org/entity/statement/Q36890893-F4E2964B-DB26-496A-A968-75D2BDE9F86F
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
P2860
Q36890893-F4E2964B-DB26-496A-A968-75D2BDE9F86F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36890893-F4E2964B-DB26-496A-A968-75D2BDE9F86F
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wasDerivedFrom
561726a26027e5eaba28a1a0757ddadb04ea50be
P2860
Mouse model reveals the role of RERE in cerebellar foliation and the migration and maturation of Purkinje cells