Molecular studies of genomic imprinting using an Angelman syndrome imprinting defect mouse model
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct neurobehavioral disorders associated with the loss of paternally or maternally expressed imprinting genes within human chromosome 15q11-q13, respectively. The human PWS/AS imprinting domain is under the control of a bipartite imprin...
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| Format: | Thesis |
| Language: | English |
| Published: |
2008
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| Online Access: | https://hdl.handle.net/10356/13578 |