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(2011) Bardet-Biedl syndrome: a study of the renal and cardiovascular phenotypes in a French cohort. Clin. J. Am. Soc. Nephrol<\/i>., 6, 22-29."},{"key":"8","unstructured":"Otto, E.A., Hurd, T.W., Airik, R., Chaki, M., Zhou, W., Stoetzel, C., Patil, S.B., Levy, S., Ghosh, A.K., Murga-Zamalloa, C.A., van Reeuwijk, J., Letteboer, S.J., Sang, L., Giles, R.H., Liu, Q., et al. (2010) Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy. Nat. Genet<\/i>., 42, 840-850."},{"key":"9","unstructured":"Saunier, S., Salomon, R. & Antignac, C. (2005) Nephronophthisis. Curr. Opin. Genet. Dev<\/i>., 15, 324-331."},{"key":"10","unstructured":"Schaefer, E., Zaloszyc, A., Lauer, J., Durand, M., Stutzmann, F., Perdomo-Trujillo, Y., Redin, C., Bennouna Greene, V., Toutain, A., Perrin, L., Gerard, M., Caillard, S., Bei, X., Lewis, R.A., Christmann, D., et al. 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