Cite
HARVARD Citation
Perrault, I. et al. (2015). IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype. Journal of medical genetics. 52 (10), pp. 657-665. [Online].
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Perrault, I. et al. (2015). IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype. Journal of medical genetics. 52 (10), pp. 657-665. [Online].