Associated Papers
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature.
Ansar M et al.
Human Molecular Genetics, 2019
CUL4-DDB1-CDT2 E3 Ligase Regulates the Molecular Clock Activity by Promoting Ubiquitination-Dependent Degradation of the Mammalian CRY1.
Tong X et al.
Plos One, 2015
The after-hours mutant reveals a role for Fbxl3 in determining mammalian circadian period.
Godinho SI et al.
Science (new York, N.y.), 2007
17463252 (PubMed )
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