Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

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Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

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Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome

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17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction

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