Changes in striatal dopamine D2 receptor binding in pre-clinical Huntington’s disease
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2008.02390.x/fullpdf
Reference23 articles.
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2. Trinucleotide repeat length and progression of illness in Huntington’s disease;Kieburtz;Journal of Medical Genetics,1994
3. Relationship between trinucleotide repeats and neuropathological changes in Huntington’s disease;Furtado;Annals of Neurology,1996
4. CAG repeat number governs the development rate of pathology in Huntington’s disease;Penney;Annals of Neurology,1997
5. [11C]raclopride-PET studies of the Huntington’s disease rate of progression: relevance of the trinucleotide repeat length;Antonini;Annals of Neurology,1998
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