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簡(jiǎn)要描述：Fragile X syndrome is the most frequent form of inherited mental retardation and is the result of transcriptional silencing of the FMR1 gene on the X chromosome. The FMR1 gene contains a distinct CpG dinucleotide repeat located in the 5' untranslated region of the gene. In fragile X syndrome this tandem repeat is substantially amplified and subjected to extensive methylation and enhanced transcriptional silencing. The FMR1 protein (or FMRP) is an RNA-binding protein that associates with pol
產(chǎn)品型號(hào)：bsm-61466R廠商性質(zhì)：生產(chǎn)廠家更新時(shí)間：2025-03-01訪 問(wèn) 量： 140產(chǎn)品分類(lèi)
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