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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主要作者: Hou, Aihua
其他作者: Chen Ken-Shiung
格式: Theses and Dissertations
語言:English
出版: 2008
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在線閱讀:https://hdl.handle.net/10356/13578
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