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De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects.

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Description scientific article published on 22 September 2017
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author: Sally L. Dunwoodie  Anne Slavotinek  Gavin Chapman  Dina Schneidman-Duhovny  David Winlaw  Kyriakie Sarafoglou  Alexander P Stegmann  Justin Szot 

Publication date December 1, 2017
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