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Browsing by Author Kartono, A.

Full Text	Issue Date	Title	Author(s)
	2009	Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.	Wijk, H.A.R.; Kersten, F.F.J.; Kartono, A.; Mans, D.A.; Brandwijk, K., et al
	2007	Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.	Arts, H.H.; Doherty, D.; Beersum, S.E.C. van; Parisi, M.A.; Letteboer, S.J.F., et al