Publication Details

Pubmed17558407
Title: Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Year: 2007
DOI: https://doi.org/10.1038/ng2069
First Author: Arts
Experimental setup: anti tag coimmunoprecipitation (UniProt)
fluorescence microscopy (UniProt)
pull down (UniProt)
two hybrid (UniProt)

Interactions

2 interactions
InteractorPartnerSourcesLink
NPHP4_HUMANFTM_HUMANUniProtdetails
FTM_HUMANFTM_HUMANUniProtdetails