Molecular BiologyCell ReportsPeer-reviewed
MAU2 and NIPBL variants in Cornelia de Lange syndrome reveal MAU2-independent loading of cohesin and uncover a protective mechanism against early truncating mutations in NIPBL
Ilaria Parenti, Farah Diab, Sara Ruiz Gil…·Kerstin S. Wendt
The paper investigates variants in MAU2 and NIPBL in CdLS, showing NIPBL haploinsufficiency as the main cause and revealing a protective mechanism for NIPBL out-of-frame mutations.
60 citationstop 3%