Associated Papers
Impaired plasma membrane localization of ubiquitin ligase complex underlies 3-M syndrome development.
Wang P et al.
The Journal of Clinical Investigation, 2019
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
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