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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Detaylı Bibliyografya
Yayımlandı:BMC Neurol
Asıl Yazarlar: Ratna, Nikhil, Kamble, Nitish L., Venkatesh, Sowmya D., Purushottam, Meera, Pal, Pramod K., Jain, Sanjeev
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Research Article
Online Erişim: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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