Endophenotypical drift in Huntington’s disease: a 5-year follow-up study

BACKGROUND: Huntington’s disease (HD) is clinically characterized by progressing motor, cognitive and psychiatric symptoms presenting as varying phenotypes within these three major symptom domains. The disease is caused by an expanded CAG repeat tract in the huntingtin gene and the pathomechanism le...

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Detalles Bibliográficos
Autores principales: Hellem, Marie N. N., Hendel, Rebecca K., Vinther-Jensen, Tua, Larsen, Ida U., Nielsen, Troels T., Hjermind, Lena E., Budtz-Jørgensen, Esben, Vogel, Asmus, Nielsen, Jørgen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336065/
https://www.ncbi.nlm.nih.gov/pubmed/34344392
http://dx.doi.org/10.1186/s13023-021-01967-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336065/
https://www.ncbi.nlm.nih.gov/pubmed/34344392
http://dx.doi.org/10.1186/s13023-021-01967-2

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