Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency

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Keywords	intellectual disability, N-terminal acetylation, NAA10, X-linked
Persistent URL	doi.org/10.1002/humu.23001, hdl.handle.net/1765/96161
Journal	Human Mutation
Organisation	Department of Clinical Genetics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Saunier, C., Støve, S. I., Popp, B., Gérard, B., Blenski, M., Ahmew, N., … Zweier, C. (2016). Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency. Human Mutation, 37(8), 755–764. doi:10.1002/humu.23001

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