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From animal models to human disease: a genetic approach for personalized medicine in ALS
Amyotrophic Lateral Sclerosis (ALS) is the most frequent motor neuron disease in adults. Classical ALS is characterized by the death of upper and lower motor neurons leading to progressive paralysis. Approximately 10 % of ALS patients have familial form of the disease. Numerous different gene mutati...
Uloženo v:
| Vydáno v: | Acta Neuropathol Commun |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4940869/ https://ncbi.nlm.nih.gov/pubmed/27400686 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-016-0340-5 |
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