Neuroectoderm phenotypes in a human stem cell model of O-GlcNAc transferase associated with intellectual disability
Author:
Funder
Novo Nordisk AS
Novo Nordisk Fonden
Wellcome Trust
Publisher
Elsevier BV
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5. O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling;Selvan;J. Biol. Chem.,2018
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