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of 3
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
Autor:
Olasz, Judit1 olasz@oncol.hu, Seidenberg, Verena2, Hummel, Susanne2, Szentirmay, Zoltán1, Szabados, György3, Melegh, Béla4, Kásler, Miklós1
Publikováno v:
Archaeological & Anthropological Sciences. Apr2019, Vol. 11 Issue 4, p1345-1357. 13p.
Publikováno v:
PLoS Genetics. Mar2008, Vol. 4 Issue 3, p1-9. 9p. 1 Diagram, 7 Graphs.