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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068943/ https://www.ncbi.nlm.nih.gov/pubmed/32164608 http://dx.doi.org/10.1186/s12883-020-01671-x |