Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.

D. Hanson, P. G. Murray, T. Coulson, A. Sud, A. Omokanye, E. Stratta, F. Sakhinia, C. Bonshek, L. C. Wilson, E. Wakeling, S. A. Temtamy, M. Aglan, E. M. Rosser, S. Mansour, A. Carcavilla, S. Nampoothiri, W. I. Khan, I. Banerjee, K. E. Chandler, G. C. BlackP. E. Clayton

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