Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

✍ Scribed by Arts, Heleen H; Doherty, Dan; van Beersum, Sylvia E C; Parisi, Melissa A; Letteboer, Stef J F; Gorden, Nicholas T; Peters, Theo A; Märker, Tina; Voesenek, Krysta; Kartono, Aileen

• Book ID: 109919589
• Publisher: Nature Publishing Group
• Year: 2007
• Tongue: English
• Weight: 565 KB
• Volume: 39
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng2069