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Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
Amyotrophic Lateral Sclerosis (ALS) is a fatal motor neuron disease presenting as sporadic (sALS) or familial (fALS) forms. Even if the list of the genes underlining ALS greatly expanded, defects in SOD1, encoding the copper/zinc superoxide dismutase
Externí odkaz:
https://doaj.org/article/9925c08dd42f49259ac0832afb43bf09