bibliographic entry 1253135 [be/1253135]
https://w3id.org/oc/corpus/be/1253135

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  • Hanson D. Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth. Am. J. Hum. Genet. 89, 148–153 (2011). PMID: 21737058
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