HAL (France)open access
A novel spliceosomopathy caused by de novo SF3B3 variants
0, SF3B3, De novo, SF3b complex, 1, All-atom simulation, Spliceosomopathy, RNA sequencing
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 312014
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.