FIGURE SUMMARY
Title

Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

Authors
Walczak-Sztulpa, J., Eggenschwiler, J., Osborn, D., Brown, D.A., Emma, F., Klingenberg, C., Hennekam, R.C., Torre, G., Garshasbi, M., Tzschach, A., Szczepanska, M., Krawczynski, M., Zachwieja, J., Zwolinska, D., Beales, P.L., Ropers, H.H., Latos-Bielenska, A., and Kuss, A.W.
Source
Full text @ Am. J. Hum. Genet.
Fig. 5

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Acknowledgments
Full text @ Am. J. Hum. Genet.
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