Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy

I. Perrault, J. Halbritter, J. Porath, X. Gerard, D. Braun, H. Gee, H. Fathy, S. Saunier, V. Cormier-Daire, S. Thomas, T. Attié-Bitach, N. Boddaert, M. Taschner, M. Schueler, E. Lorentzen, R. Lifton, E. Otto, P. Bastin, J. Kaplan, F. HildebrandtJ. M. Rozet

Research output: Contribution to journalArticle

Original languageEnglish
Article numberP7
JournalCilia
Issue numberSUPPLEMENT 1
DOIs
Publication statusPublished - 2015 Jul 13

All Science Journal Classification (ASJC) codes

  • Cell Biology

Cite this

Perrault, I., Halbritter, J., Porath, J., Gerard, X., Braun, D., Gee, H., Fathy, H., Saunier, S., Cormier-Daire, V., Thomas, S., Attié-Bitach, T., Boddaert, N., Taschner, M., Schueler, M., Lorentzen, E., Lifton, R., Otto, E., Bastin, P., Kaplan, J., ... Rozet, J. M. (2015). Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Cilia, (SUPPLEMENT 1), [P7]. https://doi.org/10.1186/2046-2530-4-S1-P7