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Publication : Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth.

First Author  Hanson D Year  2011
Journal  Am J Hum Genet Volume  89
Issue  1 Pages  148-53
PubMed ID  21737058 Mgi Id 
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