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De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features
scientific article published on 19 May 2020
Author/s
author: Julien Buratti, C Geoffrey Woods, Tamar Harel, Delphine Héron
Work details
Publication date
May 19, 2020
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Language
English
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