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References
ORIGINAL RESEARCH PAPERS
Otto, E. A. et al. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left–right axis determination. Nature Genet. 20 July 2003 (10.1038/ng1217)
Olbrich, H. et al. Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. Nature Genet. 20 July 2003 (10.1038/ng1216)
FURTHER READING
Vainio, S. & Lin, Y. Coordinating early kidney development: lessons from gene targetting. Nature Rev. Genet. 3, 533–543 (2002)
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Skipper, M. Flushing out the connections. Nat Rev Genet 4, 674–675 (2003). https://doi.org/10.1038/nrg1171
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DOI: https://doi.org/10.1038/nrg1171
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