Mitochondrial genome study in blood of maternally inherited ALS cases.

Although it did not reach statistical significance, we found a strong association in higher numbers of point mutations in ND5, a subunit of NADH dehydrogenase (complex I of the respiratory chain), in maternally linked samples compared to non-maternally linked samples when analyzing the individual point mutations by gene in whole blood (Fig. 3 d; Mann–Whitney test, p = 0.0706).

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