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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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| Publicado no: | Mol Syndromol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2020
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| Assuntos: | |
| Acesso em linha: | 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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