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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
scientific article
Author/s
author: Philip G. Murray, Jill E. Urquhart, Peter E. Clayton, Graeme Black
Work details
Publication date
July 7, 2011
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Language
English
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