Functional Study of the Imprinted Magel2 and Ndn Genes within the Prader-Willi Region
碩士 === 國立陽明大學 === 遺傳學研究所 === 90 === Prader-Willi syndrome (PWS) is a complex neurobehavioral disorder. It is known human chromosome 15q11-13 is the critical region for PWS. Loss of the paternally expressed genes within this region caused PWS phenotypes. Targeted mutagenesis of many mouse...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2002
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| Online Access: | http://ndltd.ncl.edu.tw/handle/57916991375788654269 |