A Phenotypic Atlas for Huntington Disease Based on Data From the Enroll-HD Cohort Study

BACKGROUND AND OBJECTIVES: The variable CAG repeat expansion in the huntingtin gene and its inverse relationship to motor dysfunction onset are fundamental features of Huntington disease (HD). However, the wider phenotype (including non-motor features) at particular CAG lengths, ages, and functional...

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Detalles Bibliográficos
Autores principales: Langbehn, Douglas R., Sathe, Swati S., Loy, Clement, Sampaio, Cristina, Mccusker, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684052/
https://www.ncbi.nlm.nih.gov/pubmed/38035176
http://dx.doi.org/10.1212/NXG.0000000000200111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684052/
https://www.ncbi.nlm.nih.gov/pubmed/38035176
http://dx.doi.org/10.1212/NXG.0000000000200111

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