Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease

Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease

Abstract Expanded CGG-repeats have been linked to neurodevelopmental and neurodegenerative disorders, including the fragile X syndrome and fragile X-associated tremor/ataxia syndrome (FXTAS). We hypothesized that as of yet uncharacterised CGG-repeat expansions within the genome contribute to human d...

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Autores principales: Dale J. Annear, Geert Vandeweyer, Ellen Elinck, Alba Sanchis-Juan, Courtney E. French, Lucy Raymond, R. Frank Kooy
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Medicine
R
Science
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Acceso en línea:https://doaj.org/article/29786ec0d65d4ef5b4913ce8a16e9316
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