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Juvenile Huntington’s disease: two case reports and a review of the literature

BACKGROUND: Huntington’s disease is a rare, autosomal dominant neurodegenerative disease characterized by motor, cognitive, and psychiatric symptoms. Usually, the disease symptoms first appear around the age of 40, but in 5–10% of cases, they manifest before the age of 21. This is then referred to a...

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Detaylı Bibliyografya
Yayımlandı:J Med Case Rep
Asıl Yazarlar: Lesinskienė, Sigita, Rojaka, Darja, Praninskienė, Rūta, Morkūnienė, Aušra, Matulevičienė, Aušra, Utkus, Algirdas
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7528384/
https://ncbi.nlm.nih.gov/pubmed/32998776
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-020-02494-7
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