A carregar...
Cystathionine γ-lyase deficiency mediates neurodegeneration in Huntington’s disease
Huntington’s disease is an autosomal dominant disease associated with a mutation in the gene encoding huntingtin (Htt) leading to expanded polyglutamine repeats of mutant Htt (mHtt) that elicit oxidative stress, neurotoxicity, and motor and behavioural changes(1). Huntington’s disease is characteriz...
Na minha lista:
| Publicado no: | Nature |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4349202/ https://ncbi.nlm.nih.gov/pubmed/24670645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature13136 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|