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Q38244379-A80B8F51-F1FA-43ED-B14F-CC26F059C484
Q38244379-A80B8F51-F1FA-43ED-B14F-CC26F059C484
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http://www.wikidata.org/entity/statement/Q38244379-A80B8F51-F1FA-43ED-B14F-CC26F059C484
Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A.
P2860
Q38244379-A80B8F51-F1FA-43ED-B14F-CC26F059C484
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38244379-A80B8F51-F1FA-43ED-B14F-CC26F059C484
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93ba26a49afb18a8b920f8ec88c0bca7c552ec9d
P2860
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling.