Cite
HARVARD Citation
Epting, D. et al. (2020). Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome. Human mutation. 41 (12), pp. 2179-2194. [Online].
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Epting, D. et al. (2020). Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome. Human mutation. 41 (12), pp. 2179-2194. [Online].