Mitochondrial encephalomyopathy caused by a novel ACAD9 mutation: a case report

Shuo Li1, Yijun Li1, Yonghua Chen2

  • 1The First Clinical Medical College of Anhui University of Chinese Medicine, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui, China.

Summary

This study identifies novel ACAD9 gene variants in a patient with mitochondrial encephalomyopathy, highlighting the importance of genetic sequencing for diagnosing complex neurological disorders.

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