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A list of all pages that have property "AnswerAExp" with value "A CGG expansion results in Fragile X syndrome due to an X-linked defect that affects methylation and expression of the ''FMR1'' gene. Fragile X syndrome is not caused by mutation in the dystrophin gene.". Since there have been only a few results, also nearby values are displayed.

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    • WBR1020  + (A CGG expansion results in Fragile X syndrome due to an X-linked defect that affects methylation and expression of the ''FMR1'' gene. Fragile X syndrome is not caused by mutation in the dystrophin gene.)
    Retrieved from "https://www.wikidoc.org/index.php/Special:SearchByProperty/:AnswerAExp/A-20CGG-20expansion-20results-20in-20Fragile-20X-20syndrome-20due-20to-20an-20X-2Dlinked-20defect-20that-20affects-20methylation-20and-20expression-20of-20the-20-27-27FMR1-27-27-20gene.-20Fragile-20X-20syndrome-20is-20not-20caused-20by-20mutation-20in-20the-20dystrophin-20gene."