In search of interventions to ameliorate motor deficits in mouse models of typical Rett syndrome
碩士 === 國立政治大學 === 神經科學研究所 === 103 === Rett Syndrome (RTT) is a neurodevelopmental disorder caused by mutations of the methyl-CpG-binding protein 2 (MECP2). Mice with deficient MeCP2 recapitulate many RTT-like motor symptoms, including hypoactivity, deficits in motor coordination, and motor learning,...
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| Format: | Others |
| Language: | zh-TW |
| Online Access: | http://ndltd.ncl.edu.tw/handle/93919819173541841567 |