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3. Splicing variants in NARS2 are associated with milder phenotypes and intra-familial variability.

4. Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice.

5. The human MSH5 (MutS Homolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage

6. Fatal heart failure associated with CoQ10 and multiple OXPHOS deficiency in a child with propionic acidemia

7. A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene

8. Letter to the Editor on a paper by Hsiao C-T, Tsai P-C, Liao Y-C, Lee Y-C, Soong B-W. C9ORF72 repeat expansion is not a significant cause of late-onset cerebellar ataxia syndrome. J Neurol Sci 2014;347:322–324.

9. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients.

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