Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to...

Journal of Molecular Endocrinology 2012 / 10 Vol. 49; Iss. 3

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

Hanson, D., Murray, P. G., Coulson, T., Sud, A., Omokanye, A., Stratta, E., Sakhinia, F., Bonshek, C., Wilson, L. C., Wakeling, E., Temtamy, S. A., Aglan, M., Rosser, E. M., Mansour, S., Carcavilla, A
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Volume:
49
Language:
english
Journal:
Journal of Molecular Endocrinology
DOI:
10.1530/JME-12-0034
Date:
October, 2012
File:
PDF, 183 KB
english, 2012
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