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

Overview of attention for article published in Cilia, July 2015
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3 Mendeley
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Title
Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy
Published in
Cilia, July 2015
DOI 10.1186/2046-2530-4-s1-p7
Authors

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 Hildebrandt, JM Rozet

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 33%
Student > Bachelor 1 33%
Researcher 1 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 67%
Unknown 1 33%