Associated Papers
Molecular mechanism of N-terminal acetylation by the ternary NatC complex.
Deng S et al.
Structure (london, England : 1993), 2021
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC et al.
Nature Genetics, 2020
32989326 (PubMed )
Supplement: 41588_2020_695_MOESM3_ESM.xlsx › Data_set_1
Targeted resequencing identifies genes with recurrent variation in cerebral palsy.
van Eyk CL et al.
Npj Genomic Medicine, 2019
31700678 (PubMed )
Supplement: 41525_2019_101_MOESM1_ESM.pdf
Identification of an alternatively spliced nuclear isoform of human N-terminal acetyltransferase Naa30.
Varland S et al.
Gene, 2018
The emerging genetic landscape of cerebral palsy.
van Eyk CL et al.
Handbook of Clinical Neurology, 2018
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