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ng2069
ng2069
https://scigraph.springernature.com/pub.10.1038/ng2069
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
P2888
Q24308692-18CF757D-32D6-48DF-834E-E97A5A35FA03
P2888
ng2069
https://scigraph.springernature.com/pub.10.1038/ng2069