Authors' response
- PMID: 33380712
- PMCID: PMC8061587
- DOI: 10.4103/0971-5916.305172
Authors' response
Conflict of interest statement
None
Comment on
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A descriptive pilot study of mitochondrial mutations & clinical phenotype in fibromyalgia syndrome.Indian J Med Res. 2019 Jan;149(1):47-50. doi: 10.4103/ijmr.IJMR_1977_16. Indian J Med Res. 2019. PMID: 31115374 Free PMC article.
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Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions.Indian J Med Res. 2020 Oct;152(4):429-430. doi: 10.4103/ijmr.IJMR_1039_19. Indian J Med Res. 2020. PMID: 33380711 Free PMC article. No abstract available.
References
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- MITOMAP: A human mitochondrial genome database. [accessed on September 20, 2020]. Available from: www.mitomap.org .
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- Ji Y, Liang M, Zhang J, Zhu L, Zhang Z, Fu R, et al. Mitochondrial ND1 variants in 1281 Chinese subjects with leber's hereditary optic neuropathy. Invest Ophthalmol Vis Sci. 2016;57:2377–89. - PubMed
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