Huntington's disease (HD) is a progressive neurodegenerative condition caused by the abnormal expansion of a polyglutamine tract in the N‐terminus of the huntingtin protein. Over the last 20 years, HD pathogenesis has been explained by the generation of N‐terminal fragments containing the polyglutamine stretch. A new study from Frederic Saudou's group now investigates the function of the C‐terminal fragments generated upon cleavage and shows that these products may also contribute to cellular toxicity in HD (El‐Daher et al , [2015][1]). [1]: #ref-2
CITATION STYLE
Jimenez‐Sanchez, M., & Rubinsztein, D. C. (2015). Huntington’s disease—the sting in the tail. The EMBO Journal, 34(17), 2215–2216. https://doi.org/10.15252/embj.201592467
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