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Q53169876-87497A4E-E48E-4B04-8E14-C5464DCB9F41
Q53169876-87497A4E-E48E-4B04-8E14-C5464DCB9F41
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http://www.wikidata.org/entity/statement/Q53169876-87497A4E-E48E-4B04-8E14-C5464DCB9F41
Lin-Gettig syndrome: Craniosynostosis expands the spectrum of the KAT6B related disorders.
P2860
Q53169876-87497A4E-E48E-4B04-8E14-C5464DCB9F41
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53169876-87497A4E-E48E-4B04-8E14-C5464DCB9F41
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wasDerivedFrom
098984c39d2d3621b701beda0e09adab6dd950f1
P2860
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.