Platelet abnormalities in Huntington’s disease

Huntington’s disease (HD) is a hereditary disorder that typically manifests in adulthood with a combination of motor, cognitive and psychiatric problems. The pathology is caused by a mutation in the huntingtin gene which results in the production of an abnormal protein, mutant huntingtin (mHtt). Thi...

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Detalles Bibliográficos
Autores principales: Denis, Hélèna L, Lamontagne-Proulx, Jérôme, St-Amour, Isabelle, Mason, Sarah L, Rowley, Jesse W, Cloutier, Nathalie, Tremblay, Marie-Ève, Vincent, Antony T, Gould, Peter V, Chouinard, Sylvain, Weyrich, Andrew S, Rondina, Matthew T, Barker, Roger A, Boilard, Eric, Cicchetti, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Neurodegeneration
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518476/
https://www.ncbi.nlm.nih.gov/pubmed/30567722
http://dx.doi.org/10.1136/jnnp-2018-318854

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518476/
https://www.ncbi.nlm.nih.gov/pubmed/30567722
http://dx.doi.org/10.1136/jnnp-2018-318854

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