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Q50459323-3A4DF819-6A3C-4335-926E-67B9A0F3A09B
Q50459323-3A4DF819-6A3C-4335-926E-67B9A0F3A09B
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http://www.wikidata.org/entity/statement/Q50459323-3A4DF819-6A3C-4335-926E-67B9A0F3A09B
Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.
P2860
Q50459323-3A4DF819-6A3C-4335-926E-67B9A0F3A09B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50459323-3A4DF819-6A3C-4335-926E-67B9A0F3A09B
rank
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wasDerivedFrom
151bedd801691d45e56d923ca97a3e3dc1753d86
P2860
SETD5 loss-of-function mutation as a likely cause of a familial syndromic intellectual disability with variable phenotypic expression.