Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases.

Neuromuscul Disord · 2012 · PMC3526786 · PMID 23182644

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did not reach statistical significanceno p-value reported

The mtDNA T8993C mutation, associated with NARP (neuropathy, ataxia, retinitis pigmentosa) and with maternally-inherited Leigh syndrome, was more common in the group without than with exercise intolerance, but the difference did not reach statistical significance.

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