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ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects
scientific article published on 27 July 2016
Author/s
author: Pierre Gressens, Vincent El Ghouzzi, Katsuhiko Shirahige, Sandrine Passemard, Alain Verloes, Séverine Drunat
Work details
Publication date
July 27, 2016
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Language
English
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