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pro vyhledávání: '"Rea Biacsi"'
Publikováno v:
PLoS Genetics, Vol 4, Iss 3, p e1000017 (2008)
Expansion of the CGG.CCG-repeat tract in the 5' UTR of the FMR1 gene to >200 repeats leads to heterochromatinization of the promoter and gene silencing. This results in Fragile X syndrome (FXS), the most common heritable form of mental retardation. T
Externí odkaz:
https://doaj.org/article/8500b6d849ac43399b6e245f549073f1