News archive for ProtMetD: Protein Modifications, Metabolism and Disease

Schematic representation of the Naa10 protein, encoding exons, domains and localization of mutations in affected males and females.

New NAA10 mutations identified in 11 girls and boys with development delays. (12.05.2016)

In recent years, several sporadic cases of NAA10 mutations have been identified in patients with varying degrees of developmental delays. In the curremt issue of Human Mutation, Svein Isungset Støve, Marina Blenski and Thomas Arnesen from the NAT-group at the Department of Molecular Biology in collaboration with geneticists from Germany, France, the Netherlands and the United States discovered... Read more