Developmental pleiotropy revealed by mosaic heterozygous Snrpb deletion underlies CCMS-like axial skeletal defects
Yanchen Dong, Eric Bareke, Marilou Paquin, Jennelle Smith, Sabrina Shameen Alam, Jacek Majewski, Loydie Anne Jerome‐Majewska
This study uses a mouse model to show that Snrpb deletion causes axial skeletal defects by disrupting p53 and RA signaling, without affecting somite patterning.
bioRxiv · Sep 3, 2026 · PreprintDevelopmental Biology