Clin Genet. 2011 Jan;79(1):45-7. doi: 10.1111/j.1399-0004.2010.01556_2.x. Epub 2010 Oct 12.

TMEM216 joins its ciliary cousins in ciliopathies.

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Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, 950 West 28th Avenue, Vancouver, BC, Canada. awang@cmmt.ubc.ca

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Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. [Nat Genet. 2010]
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.Valente EM, Logan CV, Mougou-Zerelli S, Lee JH, Silhavy JL, Brancati F, Iannicelli M, Travaglini L, Romani S, Illi B, et al. Nat Genet. 2010 Jul; 42(7):619-25. Epub 2010 May 30.

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TMEM216 joins its ciliary cousins in ciliopathies.
TMEM216 joins its ciliary cousins in ciliopathies.
Clin Genet. 2011 Jan ;79(1):45-7. doi: 10.1111/j.1399-0004.2010.01556_2.x. Epub 2010 Oct 12 .

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