Current research into ALS care are concentrating on several varied approaches . These include hereditary therapy , which tries to repair the defective genes causing the illness , as well as medicinal development targeting unique compounds implicated in motor neuron loss. Additionally , clinical test

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His experiments verified this therapy method works in mice for a particular mutation of the SOD1 protein associated with familial ALS. In about 50% of all ALS cases there won't be any mutations in SOD1, nevertheless the protein remains getting harmed seeking to protect the cell from totally free rad