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MAU2 and NIPBL variants in Cornelia de Lange syndrome rev... | ResearchHub
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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
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Authors
Ilaria Parenti
19 more
Ilaria Parenti
•
Farah Diab
17 more
•
Kerstin Wendt
Published
December 2, 2018
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Preprint Server
Topics
Biology
Molecular Biology
Molecular Biology
Cohesin
Haploinsufficiency
Show all topics
DOI
10.1101/477752
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Molecular Biology
Molecular Biology
Cohesin
Haploinsufficiency
Show all topics
DOI
10.1101/477752
License
cc-no
