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Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes
In its expanded form, the fragile X triplet repeat at Xq27.3 gives rise to the most common form of inherited mental retardation, fragile X syndrome. This high population frequency persists despite strong selective pressure against mutation-bearing chromosomes. Males carrying the full mutation rarely...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Wiley Subscription Services, Inc., A Wiley Company
2007
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2683060/ https://ncbi.nlm.nih.gov/pubmed/17674408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.20600 |
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