NEUROPATHOLOGICAL COMPARISON OF ADULT ONSET AND JUVENILE HUNTINGTON’S DISEASE WITH CEREBELLAR ATROPHY: A REPORT OF A FATHER AND SON

BACKGROUND: Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by a trinucleotide (CAG) repeat expansion in huntingtin (HTT) on chromosome 4. Anticipation can cause longer repeat expansions in children of HD patients. Juvenile Huntington’s disease (JHD), defined as H...

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Bibliografiset tiedot
Julkaisussa:J Huntingtons Dis
Päätekijät: Latimer, Caitlin S., Flanagan, Margaret E., Cimino, Patrick J., Jayadev, Suman, Davis, Marie, Hoffer, Zachary S., Montine, Thomas J., Gonzalez-Cuyar, Luis F., Bird, Thomas D., Keene, C. Dirk
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5832043/
https://ncbi.nlm.nih.gov/pubmed/29036832
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JHD-170261
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