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Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.

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author: Jean-Louis Mandel  Clarisse Baumann  Julien Thevenon  Christine Francannet  Amélie Piton  Claire Redin  Sandrine Passemard  Séverine Drunat 

Publication date April 29, 2015
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