Late-onset Huntington’s disease with 40–42 CAG expansion

INTRODUCTION: Huntington’s disease (HD) is a rare autosomal dominant neurodegenerative disorder caused by a CAG expansion greater than 35 in the IT-15 gene. There is an inverse correlation between the number of pathological CAG and the age of onset. However, CAG repeats between 40 and 42 showed a wi...

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Detalles Bibliográficos
Autores principales: Capiluppi, Elisa, Romano, Luca, Rebora, Paola, Nanetti, Lorenzo, Castaldo, Anna, Gellera, Cinzia, Mariotti, Caterina, Macerollo, Antonella, Cislaghi, M. Giuliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160095/
https://www.ncbi.nlm.nih.gov/pubmed/31820322
http://dx.doi.org/10.1007/s10072-019-04177-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160095/
https://www.ncbi.nlm.nih.gov/pubmed/31820322
http://dx.doi.org/10.1007/s10072-019-04177-8

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