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HARVARD Citation
Doherty, D. et al. (2010). Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis). Journal of medical genetics. 47 (1), pp. 8-21. [Online].
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Doherty, D. et al. (2010). Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis). Journal of medical genetics. 47 (1), pp. 8-21. [Online].