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| Title | Author/Creator | Date | Full Text | Reviewed | |
|---|---|---|---|---|---|
| Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks | Kerzendorfer, Claudia; Whibley, Annabel; Carpenter, Gillian; Outwin, Emily; Chiang, Shih-Chieh... More | 2010 | — | 
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| SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome | Gilfillan, Gregor D.; Selmer, Kaja K.; Sjøholm, Hans; Server, Andres; Samuelsson, Lena... More | 2008 | — |
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Author/Creator
- Carpenter, Gillian (1)
- Chiang, Shih-Chieh (1)
- Christianson, Arnold (1)
- Edkins, Sarah (1)
- Egeland, Thore (1)
- Eiklid, Kristin (1)
Keyword
- Angelman syndrome (1)
- CUL4A (1)
- CUL4B (1)
- X-linked mental retardation (XLMR) (1)
- mutations (1)
- pathogenesis (1)
