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Q50459323-A6C2EC2A-9C16-4956-94BE-B5CE98F0A41B
Q50459323-A6C2EC2A-9C16-4956-94BE-B5CE98F0A41B
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http://www.wikidata.org/entity/statement/Q50459323-A6C2EC2A-9C16-4956-94BE-B5CE98F0A41B
Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.
P2860
Q50459323-A6C2EC2A-9C16-4956-94BE-B5CE98F0A41B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50459323-A6C2EC2A-9C16-4956-94BE-B5CE98F0A41B
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Statement
wasDerivedFrom
151bedd801691d45e56d923ca97a3e3dc1753d86
P2860
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B