The establishment of diagnosis procedure and the study of CTG trinucleotide expansion pathway of myotonic dystropy
碩士 === 中山醫學院 === 醫學研究所 === 87 === Myotonic dystrophy (DM) is caused by a CTG trinucleotide expansion mutation at exon 15 of the myotonic dystrophy protein kinase (DMPK) gene. The clinical severity of this disease correlates with the length of the CTG trinucleotide repeats as well as the a...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
1999
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| Online Access: | http://ndltd.ncl.edu.tw/handle/91898306566538648923 |