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Abstract Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease affecting motor neurons in the motor cortex, brainstem, and the spinal cord
SLC25A11) and the dicarboxylate carrier (DIC
Successful biotinylation was confirmed by intact MS (performed in the MPIB MS Core Facility)
The most effective treatment is the use of low-dose of corticosteroids of 2030 mg for 35 days
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