Nyhetsarkiv for ProtMetD: Proteinmodifisering, metabolisme og sykdom
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... Les mer
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