Study of pathogfenic effects of expanded CTG trinucleotide repeats on the muscle function of C. elegans
碩士 === 中山醫學大學 === 醫學研究所 === 90 === Expansion mutation of CTG repeat length in the 3’-untranslated region of human DMPK gene causes a dominantly inherited muscular disease, called myotonic dystrophy type1 (DM1). In this study we attempt to establish a DM1-disease animal model using transge...
| 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/88412193524330023008 |