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The P42 peptide and Peptide-based therapies for Huntington’s disease

Huntington’s disease (HD) is a progressive neurodegenerative hereditary disease clinically characterised by the presence of involuntary movements, behavioural problems and cognitive decline. The disease-onset is usually between 30 and 50 years of age. HD is a rare disorder affecting approximately 1....

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Orphanet J Rare Dis
Egile Nagusiak: Marelli, Cecilia, Maschat, Florence
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2016
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4794846/
https://ncbi.nlm.nih.gov/pubmed/26984770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0405-3
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