De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects
Resource Type
Journal
Authors
Slavotinek, Anne ; Risolino, Maurizio ; Losa, Marta ; Cho, Megan T. ; Monaghan, Kristin G. ; Schneidman-Duhovny, Dina ; Parisotto, Sarah ; Herkert, Johanna C. ; Stegmann, Alexander P. A. ; Miller, Kathryn ; Shur, Natasha ; Chui, Jacqueline ; Muller, Eric ; DeBrosse, Suzanne ; Szot, Justin O. ; Chapman, Gavin ; Pachter, Nicholas S. ; Winlaw, David S. ; Mendelsohn, Bryce A. ; Dalton, Joline ; Sarafoglou, Kyriakie ; Karachunski, Peter I. ; Lewis, Jane M. ; Pedro, Helio ; Dunwoodie, Sally L. ; Selleri, Licia ; Shieh, Joseph
Source
HUMAN MOLECULAR GENETICS ; DEC 15 2017, 26 24, p4849-p4860, 12p.
Subject
Language
English
ISSN
14602083