No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50

The 5′ untranslated region of the fragile X mental retardation gene, FMR1, contains a polymorphic CGG repeat. Expansions of this repeat are associated with a spectrum of disorders. Full mutation alleles, repeats ≥ 200, are associated with fragile X syndrome. Premutation alleles, repeats of ∼55–199,...

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Detalhes bibliográficos
Main Authors: Hunter, Jessica Ezzell, Allen, Emily Graves, Abramowitz, Ann, Rusin, Michele, Leslie, Mary, Novak, Gloria, Hamilton, Debra, Shubeck, Lisa, Charen, Krista, Sherman, Stephanie L.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2668066/
https://ncbi.nlm.nih.gov/pubmed/19026394
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.10.021
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