Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth
Title:
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:
Hanson, Dan Murray, Philip G. O'Sullivan, James Urquhart, Jill Daly, Sarah Bhaskar, Sanjeev S. Biesecker, Leslie G. Skae, Mars Smith, Claire Cole, Trevor Kirk, Jeremy Chandler, Kate Kingston, Helen Donnai, Dian Clayton, Peter E. Black, Graeme C.M.