Cite
HARVARD Citation
Perrault, I. et al. (2015). Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Cilia. 4 (1), p. 1. [Online].
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Perrault, I. et al. (2015). Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Cilia. 4 (1), p. 1. [Online].