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Extending the Phenotypic Spectrum of Huntington Disease: Hypothermia
Huntington disease (HD) is an autosomal dominant progressive neurodegenerative disorder associated with expanded CAG repeat size in the huntingtin gene and usually presenting with movement disorder, psychiatric symptoms, and cognitive decline. Sleep problems, weight loss, and cachexia are also commo...
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| Pubblicato in: | Mol Syndromol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
S. Karger AG
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7109404/ https://ncbi.nlm.nih.gov/pubmed/32256303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000505887 |
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