Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.
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Valente EM, et al. Among authors: shalev s.
Nat Genet. 2010 Jul;42(7):619-25. doi: 10.1038/ng.594. Epub 2010 May 30.
Nat Genet. 2010.
PMID: 20512146
Free PMC article.