Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationEdgar A. Otto, Friedhelm Hildebrandt, Karl S. Hiller et al.|Nature Genetics|2003Cited by 643
A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in EvolutionEdgar A. Otto, Friedhelm Hildebrandt, Julia Hoefele et al.|The American Journal of Human Genetics|2002Cited by 210