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FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature www.medrxiv.org/content/10.1101/2024.09.28.24314530v1
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature https://www.medrxiv.org/content/10.1101/2024.09.28.24314530v1
FBXO22 encodes an F-box protein which acts as a substrate-recognition component of the SKP1-CUL1-F-b
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medRxivpreprint
@medrxivpreprint.bsky.social
297 followers0 following13k posts