https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:9647 Sat 24 Mar 2018 08:35:25 AEDT ]]> SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:5320 Sat 24 Mar 2018 07:45:58 AEDT ]]>