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Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 2, p 904 (2021)
Amyotrophic lateral sclerosis (ALS) is a devastating adult-onset neurodegenerative disease characterized by the progressive degeneration of upper and lower motoneurons. Most ALS cases are sporadic but approximately 10% of ALS cases are due to inherit
Externí odkaz:
https://doaj.org/article/dc526b882d034a67b803086a1df43098