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Pharmacogenomics and Personalized Medicine Volume 17, 2024 - Issue
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LETTER

Mitochondrial Diabetes May Not Be the Only Phenotypic Presentation of the m.5826A>G mtDNA Variant [Letter]

Josef FinstererNeurology & Neurophysiology Center, Vienna, AustriaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0003-2839-7305View further author information
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Pages 401-402 | Received 02 Jun 2024, Accepted 23 Jul 2024, Published online: 24 Jul 2024

References

  • Li X, Shang J, Li S, Wang Y. Identification of a novel mitochondrial tRNA mutation in Chinese family with type 2 diabetes mellitus. Pharmgenomics Pers Med. 2024;17:149–161. doi:10.2147/PGPM.S438978
  • Seo JS. Chronological change of left ventricular global longitudinal strain in patients with maternally inherited diabetes and deafness: a case series. Medicine. 2024;103(10):e37447. doi:10.1097/MD.0000000000037447
  • Yang L, Guo Q, Leng J, Wang K, Ding Y. Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutations. J Clin Lab Anal. 2022;36(1):e24102. doi:10.1002/jcla.24102
  • Matsumoto J, Saver JL, Brennan KC, Ringman JM. Mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS). Rev Neurol Dis. 2005;2(1):30–34.

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