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ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects

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Description scientific article published on 27 July 2016
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author: Alain Verloes  Pierre Gressens  Vincent El Ghouzzi  Sandrine Passemard  Katsuhiko Shirahige  Séverine Drunat 

Publication date July 27, 2016
Language English
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