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Psychiatric morbidity and poor follow-up underlie suboptimal functional and survival outcomes in Huntington’s disease
BACKGROUND: Huntington’s disease (HD), an inherited, often late-onset, neurodegenerative disorder, is considered to be a rare, orphan disease. Research into its genetic correlates and services for those affected are inadequate in most low-middle income countries, including India. The apparent ‘incur...
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| Publicado no: | BMC Neurol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7068943/ https://ncbi.nlm.nih.gov/pubmed/32164608 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-020-01671-x |
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