Associated Papers
Structure of CRL7FBXW8 reveals coupling with CUL1-RBX1/ROC1 for multi-cullin-RING E3-catalyzed ubiquitin ligation.
Hopf LVM et al.
Nature Structural & Molecular Biology, 2022
The 3M syndrome.
Huber C et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2011
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
Huber C et al.
European Journal of Human Genetics : Ejhg, 2009
Identification of mutations in CUL7 in 3-M syndrome.
Huber C et al.
Nature Genetics, 2005
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