Disruption of a Ciliary B9 Protein Complex Causes Meckel Syndrome

William E. Dowdle, Jon F. Robinson, Andreas Kneist, M. Salome Sirerol-Piquer, Suzanna G. M. Frints, Kevin C. Corbit, Norran A. Zaghloul, Gesina van Lijnschoten, Leon Mulders, Dideke E. Verver, Klaus Zerres, Randall R. Reed, Tania Attie-Bitach, Colin A Johnson, Jose Manuel Garcia-Verdugo, Nicholas Katsanis, Carsten Bergmann, Jeremy E. Reiter

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)94-110
JournalAmerican Journal of Human Genetics
Issue number1
Publication statusPublished - 15 Jul 2011

Cite this

Dowdle, W. E., Robinson, J. F., Kneist, A., Salome Sirerol-Piquer, M., Frints, S. G. M., Corbit, K. C., Zaghloul, N. A., van Lijnschoten, G., Mulders, L., Verver, D. E., Zerres, K., Reed, R. R., Attie-Bitach, T., Johnson, C. A., Manuel Garcia-Verdugo, J., Katsanis, N., Bergmann, C., & Reiter, J. E. (2011). Disruption of a Ciliary B9 Protein Complex Causes Meckel Syndrome. American Journal of Human Genetics, 89(1), 94-110. https://doi.org/10.1016/j.ajhg.2011.06.003