Studies of The Methylation of The FMR-1 Product FMRP and Screening of Fragile X patients by Western Blot Analysis
碩士 === 中山醫學院 === 醫學研究所 === 85 === Fragile X syndrome is the most common cause of inherited mental retardation. Loss of function of the FMR-1 gene appearsto result in the disease. The physiological function of FMR-1 protein (FMRP) pr...
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| Format: | Others |
| Language: | zh-TW |
| Online Access: | http://ndltd.ncl.edu.tw/handle/28566555825165562348 |