Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects
Ogden 综合征的生化和细胞分析揭示了下游 Nt 乙酰化缺陷
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddu611
Line M Myklebust, Petra Van Damme, Svein I Støve, Max J Dörfel, Angèle Abboud, Thomas V Kalvik, Cedric Grauffel, Veronique Jonckheere, Yiyang Wu, Jeffrey Swensen, Hanna Kaasa, Glen Liszczak, Ronen Marmorstein, Nathalie Reuter, Gholson J Lyon, Kris Gevaert, Thomas Arnesen