NAA20

Publications

D'Onofrio G et al. Novel biallelic variants expand the phenotype of NAA20-related syndrome. Clin Genet. 2023;104(3):371-376. PMID: 37191084.

Morrison J et al. Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly. Genet Med. 2021;23(11):2213-2218. PMID: 34230638.