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EAAT2 and the molecular signature of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a rapid and fatal neurodegenerative disease, primarily affecting upper and lower motor neurons. It is an extremely heterogeneous disease in both cause and symptom development and its mechanisms of pathogenesis remain largely unknown. Excitotoxicity, a process c...
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| Publicado no: | Adv Neurobiol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6668619/ https://ncbi.nlm.nih.gov/pubmed/28828608 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-319-55769-4_6 |
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