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Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

Author:

Dan Hanson,Philip G. Murray,James O'Sullivan,Jill Urquhart,Sarah Daly,Sanjeev S. Bhaskar,Leslie G. Biesecker,Mars Skae,Claire Smith,Trevor Cole,Jeremy Kirk,Kate Chandler,Helen Kingston,Dian Donnai,Peter E. Clayton,Graeme C.M. Black

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

15 July 2011

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