Genetic contributions to mitochondrial dysfunction in amyotrophic lateral sclerosis etiology.

HGG Adv · 2026 · PMC13147394 · PMID 41966055

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a notable trendno p-value reported

Further investigation of individuals with ALS carrying a variant in a mtDNA maintenance gene, including POLG , revealed a notable trend relating to the reported site of symptom onset.

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