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Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.
scientific article
Author/s
author: Julien Thevenon, Amélie Piton, Sandrine Passemard, Séverine Drunat, Jean-Louis Mandel, Clarisse Baumann, Claire Redin, Christine Francannet
Work details
Publication date
April 29, 2015
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Language
English
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