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Comment
. 2020 Oct;152(4):429-430.
doi: 10.4103/ijmr.IJMR_1039_19.

Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions

Josef Finsterer  1
Affiliations
Comment

Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions

Josef Finsterer. Indian J Med Res. 2020 Oct.
No abstract available

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Conflict of interest statement

None

Comment in

  • Authors' response.
    Danda S, Thomas BM, Paramshivam G, Thomas R, Mathew J, Danda D. Danda S, et al. Indian J Med Res. 2020 Oct;152(4):430-431. doi: 10.4103/0971-5916.305172. Indian J Med Res. 2020. PMID: 33380712 Free PMC article. No abstract available.

Comment on

References

    1. Danda S, Thomas BM, Paramasivam G, Thomas R, Mathew J, Danda D. A descriptive pilot study of mitochondrial mutations & clinical phenotype in fibromyalgia syndrome. Indian J Med Res. 2019;149:47–50. - PMC - PubMed
    1. Finsterer J, Milvay E. Lactate stress testing in 155 patients with mitochondriopathy. Can J Neurol Sci. 2002;29:49–53. - PubMed
    1. Pennisi EM, Garibaldi M, Antonini G. Lipid myopathies. J Clin Med. 2018;7:E472. - PMC - PubMed
    1. Nesti C, Rubegni A, Tolomeo D, Baldacci J, Cassandrini D, D'Amore F, et al. Complex multisystem phenotype associated with the mitochondrial DNA m.5522G>A mutation. Neurol Sci. 2019;40:1705–8. - PubMed
    1. Poulton J, Finsterer J, Yu-Wai-Man P. Genetic counselling for maternally inherited mitochondrial disorders. Mol Diagn Ther. 2017;21:419–29. - PubMed

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