bibliographic entry 12848470 [be/12848470]
https://w3id.org/oc/corpus/be/12848470
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Arts, HH. Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome, Nat Genet, 2007, 39, 882, 8, PMID: 17558407
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