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| Title | Author/Creator | Date | Full Text | Reviewed | |
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| Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families | Hynes, Kim; Tarpey, Patrick; Haan, Eric; Turner, Gillian; Christodoulou, John... More | 2010 | — | 
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| Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans | Wu, Ye; Arai, Amy C.; Boyle, Jackie; Tarpey, Patrick; Raymond, F. Lucy... More | 2007 | — |
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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
- Raymond, F. Lucy (2)
- Smith, Raffaella (2)
- Stratton, Michael R. (2)
- Al Raisi, Zahyia (1)
- Arai, Amy C. (1)
- Bayly, Marta A. (1)
- Berkovic, Samuel F. (1)
Keyword
- AMPA (1)
- Angelman syndrome (1)
- DNA (1)
- GRIA3 (1)
- PCDH19 mutations (1)
- X-linked mental retardation (XLMR) (1)
- cognitive impairment (1)
- epilepsy (1)
- females (1)
- heteromeric receptors (1)
