Cheng H et al. Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15. Hum Mol Genet. 2020;29(5):877-878. PMID: 32027362.
Saunier C et al. Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency. Hum Mutat. 2016;37(8):755-64. PMID: 27094817.
Wu Y et al. NAA10-related syndrome. Exp Mol Med. 2018;50(7):1-10. PMID: 30054457.
Myklebust LM et al. Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects. Hum Mol Genet. 2015;24(7):1956-76. PMID: 25489052.
Rope AF et al. Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency. Am J Hum Genet. 2011;89(1):28-43. PMID: 21700266.