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Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
PURPOSE: Fragile X syndrome, the most common inherited form of human mental retardation, arises as a consequence of a large expansion of a CGG trinucleotide repeat in 5′ untranslated region of the fragile X mental retardation 1 (FMR1) gene located on the X chromosome. Although the FMR1 gene was clon...
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| Pubblicato in: | Genet Med |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2007
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5453801/ https://ncbi.nlm.nih.gov/pubmed/17666893 |
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