The role of SIGMAR1 gene mutation and mitochondrial dysfunction in amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) patients exhibit diverse pathologies such as endoplasmic reticulum (ER) stress and mitochondrial dysfunction in motor neurons. Five to ten percent of patients have familial ALS, a form of the disease caused by mutations in ALS-related genes, while sporadic forms o...
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Elsevier,
2015-01-01T00:00:00Z.
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A1234.567 |
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