Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth
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| Description | scientific article |
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author: Philip G. Murray Jill E. Urquhart Peter E. Clayton Graeme Black |
| Publication date | July 7, 2011 |
| Language | English |
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